Synthesis of Oxycodone from Codeine[ Back to the Chemistry Archive ] Method #1 [1]Codeine to codeinone To a solution of dimethylsulfoxide (16.53 g, 0.21 mole) in CH2Cl2 (80 ml) at -78°C was added dropwise a solution of oxalyl chloride (13.01 g, 0.10 mole) in CH2Cl2 (50 ml) over a period of 40 min. After stirring for 10 min., a solution of codeine (20.33 g, 0.068 mole) in CH2Cl2 (100 ml) was added over 50 min. while keeping the reaction mixture at -78°C. After stirring at -78°C for 2 hr., Et3N (50 ml) was added, followed by CH2Cl2 (100 ml). The reaction mixture was allowed to warm-up to room temperature, washed with water (6 x 150 ml), dried over anhydrous Na2SO4 and evaporated to dryness in vacuo to give codeinone (25.57 g). Codeinone to codeinone dienol acetate A mixture of codeinone (5.98 g, 0.02 mole), sodium acetate (1.77 g, 0.02 mole) and acetic anhydride (35.76 g, 0.35 mole) in toluene (6 ml) was heated at 90°C about 105°C for 5 hr, cooled, diluted with CH2Cl2 (300 ml), and basified with NaHCO3 (66 g in 300 ml of ice-cold water). The organic portion was separated, washed with water (4 x 150 ml), dried over anhydrous Na2SO4, and evaporated to dryness in vacuo to give an oil (9.4 g), which was chromatographed on silica gel with 5% CH3OH in CH2Cl2 to give codeinone dienol acetate as brown needles (5.62 g, 83% yield) Codeinone dienol acetate to Oxycodone A solution of codeinone dienol acetate (0.50 g, 1.48 mmol), formic acid (0.7 ml), hydrogen peroxide (0.43 g, 30%, 3.79 mmol), and water (1.4 ml) was heated at 43-44°C for 6 hr and cooled to rt. over night. To the solution was added 5% Pd/C (80 mg) and hydrogenated at rt. under 28 psi of hydrogen gas for 18 hr. The reaction mixture was filtered. The filtrate was basified with NH4OH and extracted with methylene chloride. The extract was washed with water, dried over anhydrous sodium sulfate, and evaporated in vacuo to dryness to give oxycodone (0.40 g, 85% yield). The Rf value in TLC and the IR spectrum of the product were comparable to those obtained from an authentic sample. Additional information Codeinone dienol acetate to 14-hydroxycodeinone with H2O2 A solution of codeinone dienol acetate (1.12 g, 3.3 mmol), formic acid (90% aqueous solution, 0.80 g, 15.6 mmol), hydrogen peroxide (31% aqueous solution, 0.90 g, 8.2 mmol), and water (1.60 g) was allowed to stir at 40-42°C for 4.5 hr, cooled to room temperature, basified with concentrated NH4OH, and extracted with CH.sub.2 Cl.sub.2 (50 ml). The extract was washed with water (20 ml), dried over anhydrous Na2SO4, and evaporated to dryness in vacuo to give 1,4-hydroxycodeinone (0.80 g, 78% yield). The Rf value in TLC, the IR spectrum and the NMR spectrum of the product were comparable to those obtained from an authentic sample. Codeinone dienol acetate to 14-hydroxycodeinone with MCPBA A solution of codeinone dienol acetate (1.16 g, 3.4 mmol), oxalic acid (0.70 g, 7.4 mmol) and 3-chloroperoxybenzoic acid (57.about.86%, 0.83 g) in glacial acetic acid (10.02 g) was allowed to stir at room temperature for 6 hr, basified with concentrated NH4OH, and extracted with CH2Cl2 (50 ml). The extract was washed with water (10 ml), dried over anhydrous Na2SO4, and evaporated to dryness in vacuo to give a crude product (1.29 g), which was chromatographed on silica gel to give pure 14-hydroxycodeinone (0.76 g, 72% yield). Codeinone to 14-hydroxycodeinone with H2O2 A solution of codeinone (0.503 g, 1.7 mmol), formic acid (0.7 ml) and H.sub.2 O.sub.2 (1.0 ml) in Water (1.4 ml) was allowed to stir at 50.degree.-55.degree. C. for 7 hr. The mixture was cooled, basified with NH.sub.4 OH, and extracted with CHCl.sub.3 (3.times.15 ml). The extract was washed with water, dried over anhydrous Na.sub.2 SO.sub.4 and evaporated to dryness in vacuo to give a solid residue (0.17 g), which is comparable to 14-hydroxycodeinone in its IR spectrum, NMR spectrum, and the R.sub.f value in TLC with those of an authentic sample.
Method #2 [2]Codeine to codeinone Codeinone was prepared by oxidation of codeine sulfate trihydrate. A reaction mixture was prepared containing codeine sulfate trihydrate (10.4 g), de-ionized water (20 g) and isopropyl acetate (87.2 g) at ambient temperature. The reaction mixture was agitated and the resultant mixture cooled to about 20(+/-)5°C Concentrated ammonium hydroxide (18.0 g) was added in several portions and the mixture was maintained at a temperature of about 20(+/-)5°C with stirring. Stirring was continued for about 15 minutes, and then a small portion of the aqueous layer was withdrawn to check for pH value, which was to be advantageously maintained between 11.0 and 12.0. The aqueous layer was then separated and re-extracted with isopropyl acetate (35 g). The combined organic layers (isopropyl acetate) were concentrated in vacuo to near dryness at temperature NMT 45.degree. C. The residual isopropyl acetate solvent was chased by adding 18 g of toluene. The concentration process was then repeated in vacuo. Codeine free base dissolved in a mixture of toluene (177 g) and cyclohexanone (47.4 g) at temperature NMT 45°C was then transferred to the reaction flask which was equipped with magnetic stirrer, thermocouple, Dean-Stark trap with condenser attached, addition funnel with an extender (about 4 inches height), and a nitrogen-inlet adapter. The mixture was heated to boiling temperature (about 116-118°C) under a nitrogen atmosphere and 26 g (30 ml) of distillate were collected in the Dean-Stark trap. A solution of aluminum isopropoxide (3.5 g) in 35.5 g (41 ml) of toluene was then added to the addition funnel. The heating rate was adjusted and the aluminum isopropoxide/toluene solution was added into the reaction mixture at such a rate that the total volume was added over a 10-20 minute period (approximately the same volume (41 ml) of distillate was collected in the Dean-Stark trap). After completion of the addition, collection of the distillate was continued such that 57 g (66 ml) of distillate was collected in the Dean-Stark trap at a similar distillation rate. The heat source was removed and the mixture allowed to cool down to ambient temperature (under nitrogen atmosphere) over a period of about 30 minutes. Reaction completeness was determined by withdrawing a small sample from the batch, extracting it with a saturated sodium bicarbonate solution and ethyl acetate, concentrating the organic layer, re-dissolving it with the HPLC mobile phase, and analyzing the sample on HPLC. The reaction was considered complete if the area % of codeine was less than 3.5A%. An aqueous solution of 13 wt. % Rochelle salt was then prepared by dissolving 19.5 g of potassium sodium tartrate tetrahydrate in 130.5 g of de-ionized water at 20(+/-)5°C. The aqueous Rochelle salt solution (90 ml) was added into the reaction mixture in one portion at ambient temperature, the batch stirred for about 10 minutes, and filtered. Both layers were saved. The organic layer was washed with 60 ml of aqueous Rochelle salt solution (both layers were saved). The organic layer was washed with a mixture of 30 ml brine solution and 30 ml 5% sodium bicarbonate solution (both layers were saved). All aqueous layers were then combined and extracted with 43 g (50 ml) of toluene. The aqueous layer was discarded. The organic layers were then combined and concentrated in vacuo at temperature NMT 55°C to near dryness. Twenty-two grams (25 ml) of toluene was added and the resultant organic layer concentrated in vacuo twice more to remove residual cyclohexanone. Subsequently, 11.8 g (15 ml) of 2-propanol was added and the mix slurried at 0-5°C for at least eight hours under a nitrogen atmosphere. Solids were then filtered and the flask/wet cake rinsed with the chilled (about 5°C) recycled filtrate. The latter operation was repeated until no solids were left in the flask. The chilled wet cake was then rinsed with chilled (5-10°C) 2-propanol (12 g, 15 ml), and filter dried. The wet cake was then rinsed with heptane (6.8 g, 10 ml) and filter-dried. The resulting solids were vacuum dried at temperature NMT 50°C to a constant weight. A yield of 5.2 to 6.45 g (65.4 to 81.2%) of off-white solids, with HPLC purity of about 96A%-99.3A% was obtained. The compound was stored in a dark and cool place. Codeinone to Dienolsilyl Ether of Codeinone Codeinone (6.0 g) with toluene (104 g) was added to a reaction flask equipped with a mechanical stirrer, thermocouple, Dean-Stark trap with condenser attached, and a nitrogen-inlet adapter. The batch was heated to reflux and about 27.7 g (32 ml) of distillate was collected in the Dean-Stark trap. The contents were then cooled to 20(+/-)5°C under a nitrogen atmosphere. A solution of DBU (4.22 g) in toluene (3 g) was added in one portion. Subsequently, a solution of t-BDMSiCl (4.22g) in toluene (5 g) was likewise added in one portion. The batch was slowly warmed to 58(+/-)3°C and stirred at this temperature for about 2 hours. Completion of the reaction was adjudged by withdrawing a small sample from the batch, extracting it with a mixture of ethyl acetate and saturated sodium bicarbonate solution, spotting the organic layer on a TLC plate, and then eluting it with a mobile phase of 9:1 mixture of dichloromethane and methanol plus 3-4 drops of concentrated ammonium hydroxide. If the reaction was determined to be incomplete, stirring was continued at 58(+/-)3°C for an additional 2 hours and a TLC check performed once more. Alternatively reaction completion was accomplished by adding about 5-10% more of both DBU and tBDMSiCl to the reaction mixture at the same temperature. The contents were then cooled to 20(+/-)5°C, and a mixture of 5% sodium bicarbonate solution (80 ml) and 60 ml of water was added in one portion. Stirring continued for about 10 minutes. The aqueous layer was then separated and discarded. The organic layer was washed with a mixture of 50 ml brine and 50 ml saturated ammonium chloride solution (the aqueous layers were discarded). The organic layer was concentrated to near dryness in vacuo at temperature NMT 50°C, and the residue diluted with 33.2 g of toluene to make up a 20 wt. % stock solution. Yield was approximately quantitative. The stock solution was found to be stable at ambient temperature under nitrogen atmosphere for at least 6 months. Dienolsilyl Ether of Codeinone to 14-hydroxycodeinone Peracetic acid solution(for prep see below) (107.7 g of 9.0 wt. % peracetic acid) at ambient temperature (22(+/-)5°C) was added to a reaction flask (3-neck, 500 ml) equipped with mechanical stirrer and thermocouple, nitrogen-inlet adapter and addition funnel. A 20 wt. % stock solution of the dienolsilyl ether of codeinone (41.7 g) was added through the addition funnel over a period of about 5 minutes and the temperature of the contents maintained at NMT 28°C The batch was stirred at 22(+/-)5°C for at least 3 hours. In order to test reaction completeness, a small sample was withdrawn from the batch and quenched with saturated sodium bicarbonate solution, and extracted with ethyl acetate. The EtOAc layer was spotted onto a TLC plate and subsequently checked for the disappearance of starting dienolsilyl ether of codeinone. The TLC mobile phase was a mixture of 95:5 of dichloromethane and methanol plus 3-5 drops of concentrated ammonium hydroxide. If the reaction was adjudged incomplete, the mixture was stirred at the same temperature for an additional 2 hours then analyzed by TLC again. Alternatively completion of the reaction was pushed by the addition of 10 g of peracetic acid (9.0 wt. %) and stirring for an additional 1 h (analysis was then once more preformed using TLC). Upon determination of the completion of the reaction 20.0 g of 10 wt. % of aqueous sodium hydrogen sulfite solution was added in one portion, and the resultant admixture stirred for 10 minutes at ambient temperature. The batch was then concentrated in vacuo at temperature NMT 45°C to dryness. Subsequently water (180 g), toluene (69 g), ethyl acetate (36 g) were added and vigorous stirring for about 10 minutes undertaken. The resulting layers were separated and the aqueous layer saved in a flask. The organic layer was washed thrice with a solution of 26 ml of 2.5% HCl. The combined aqueous layers were then filtered through a pad of wet (with water) hyflo-supercel filter aid. Subsequently, EtOAc (85 g) was added to the filtrate and concentrated ammonium hydroxide added in a quantity to adjust the pH of the aqueous layer to about 11. The mixture was stirred for 10 minutes at about 60°C and the layers were separated and saved. The aqueous layer was washed with EtOAc (50g) and then discarded. The combined organic layers were concentrated in vacuo to dryness at temperature NMT 50°C To the residue was added 2-propanol (13 g), and the resultant mixture stirred at 5-10C for at least 5 hours. The solids were filtered, the flask and solids rinsed with the chilled (5°C) filtrate followed by chilled (5-10°C) 2-propanol (10 g) and heptane (8 g). The solid was then vacuum dried at temperature NMT 50°C to a constant weight. A yield of between 3.50-4.96 g (55%-78%) of 14-hydroxycodeinone free base with a purity of over 96A % was obtained. Making Peracetic Acid 14-Hydroxycodeinone was synthesized from the dienolsilyl ether of codeinone by oxidative hydroxylation using a peracetic acid solution preparation. The peracetic acid solution was prepared as follows: Acetic anhydride (80.0 g) and concentrated sulfuric acid (0.15 g, or about 6 drops) at ambient temperature were added to a clean and dried round bottom flask (3-neck, 250 ml) equipped with mechanical stirrer, thermocouple, nitrogen-inlet adapter and addition funnel. The mixture was cooled to about 10.+.3°C under a nitrogen atmosphere. A 14.0 g of 30% aqeous hydrogen peroxide solution was slowly added through the addition funnel. The addition of hydrogen peroxide was performed drop by drop maintaining content temperature at NMT 27.degree. C. (formation of peracetic acid and the hydrolysis of acetic anhydride are strongly exothermic, cooling is absolutely essential, but over-chilling the batch is not recommended). After complete addition, the batch was stirred for about 30 minutes in a 10(+/-)3°C bath. Acetic acid (10.0 g) was then added through the addition funnel, and the batch slowly warmed to 25(+/-)5°C The batch was then stirred for an additional hour (the batch should be kept in water bath all the time in order to avoid any unexpected exotherm). Oxycodone from 14-Hydroxycodeinone By Catalytic Hydrogenation 14-Hydroxycodeinone (4.98 g) and acetic acid (155 g) were added to a Parr shaker equipped with hydrogen inlet and outlet connectors. The mixture was shaken for about 5 minutes to completely dissolve the 14-hydroxycodeinone at ambient temperature. The system was then evacuated and the Parr shaker was filled with nitrogen. In one portion, under the nitrogen atmosphere, 10% Pd/C (50% water wet, 4.0 g) was added. The system was then evacuated, and was filled with hydrogen gas to a pressure of about 38 psi. The hydrogen inlet from the supply tank was then closed and the mixture was shaken at an initial pressure of 38 psi for about 3 hours (at ambient temperature). After 3 hours of shaking, the system was evacuated and filled with nitrogen. The contents were filtered over a hyflo-supercel filtering pad (3 g, wetted with water). The Parr bottle and wet cake were then rinsed with acetic acid (2 x 21 g). The filtrate was concentrated in vacuo to dryness at temperature NMT 50°C The residue was then dissolved with de-ionized water (50 g), and the pH adjusted to about 11.0 to 12.0 using 20% aqueous KOH solution and concentrated ammonium hydroxide (4 g). The mixture was then extracted with ethyl acetate (4 x 135 g), and the combined organic layers concentrated in vacuo to dryness. A yield of 3.51 to 4.26 g of crude oxycodone with HPLC purity of over 85A% (70.0 to 85.0% yield) was obtained. Oxycodone from 14-Hydroxycodeinone By Catalytic Transfer Hydrogenation Method 14-Hydroxycodeinone (4.98 g) and acetic acid (137 g) were added to a reaction flask (3-neck, 250 ml) equipped with mechanical stirrer, addition funnel, thermocouple and nitrogen-inlet adapter. The system was evacuated and the flask filled with nitrogen. Subsequently, 5% Pd/C (50% water wet, 3.0 g) in one portion was added under the nitrogen atmosphere. While the mixture was stirred for about 5 minutes at ambient temperature (22(+/-)5°C), a solution of sodium hypophosphite (6.0 g) in de-ionized water (25 g) was prepared. The aqueous sodium hypophosphite solution was transferred into the addition funnel, and added to the reaction mixture over a period of about 30 minutes with maintenance of content temperature at about 22(+/-)5°C The mixture was then warmed to about 45°C and stirred for about 1 hour. To determine the completeness of the reaction, a small sample was withdrawn from the batch and the sample was filtered by means of a syringe filter into a mixture of ethyl acetate and saturated sodium bicarbonate solution. After extraction, the organic layer was concentrated to dryness and the residue dissolved with HPLC mobile phase. The disappearance of 14-hydroxycodeinone was determined. If the reaction was discerned to be incomplete, the batch was stirred for an additional 2 h period at 45°C, and the HPLC check performed once more. Upon determination that the reaction was complete, the batch was cooled to ambient temperature (22(+/-)5°C) under the nitrogen atmosphere, and the contents filtered over a hyflo-supercel filtering pad (3.0 g, wetted with water). The flask and wet cake were rinsed with acetic acid (20 g). The filtrate was concentrated in vacuo to near dryness at temperature NMT 50°C The residue was dissolved with de-ionized water (50 g) and the pH adjusted to 11.0 to 12.0 with 20% aqueous KOH solution and concentrated ammonium hydroxide (about 4 g). The mixture was then extracted with ethyl acetate (4 x 135 g) and the combined organic layers concentrated to dryness in vacuo. Crude oxycodone with an HPLC purity of over 85% was obtained in a yield of 70.0 to 85.0% (3.51 to 4.26 g). Method #3 [3]Codeine to codeinone Codeinone was prepared by oxidation of codeine phosphate or
codeine. A solution of codeine or codeine phosphate was dissolved in the
appropriate solvent system and a specified volume of hydrochloric acid of
varying concentration was added. Manganese dioxide (freshly prepared
gamma-manganese dioxide) was added and the reaction mixture was stirred at
ambient temperature for 1.5 to 4 hours. The progress of the reaction was
monitored by HPLC. The reaction mixture was filtered through a celite pad,
washed with additional solvent or water, and neutralized with ammonium
hydroxide. The product was extracted with methylene chloride (3 x 150 ml) and
the combined extracts washed with water and dried over anhydrous sodium sulphate.
The organic layer was then evaporated to yield codeinone. The results can
be seen in the following table.
Preparation of gamma-Manganese Dioxide Manganese (II) sulphate monohydrate (140 g) was dissolved in
2.66 liters of water and heated to 60°C. Potassium permanganate (97.3 g) in
1.85 liter of water was added over a period of 15 minutes and stirred at 60°C
for 1 hour, until manganese dioxide precipitated out. The reaction mixture was
filtered and the residue was washed with deionised water until no sulphate ion
was present. The solid was dried under suction for 2 hours followed by drying at
70°C under vacuum to a constant weight (about 8 days) to give 115 g of a dark
brown powder. References [1] US Pat. 5,869,669
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