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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968377Generated: October 29, 2026

Methanol → Thebaine

https://huagongshe.com/reaction/968377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantMethanesulfonic AcidHCID 6395—
ReactantTrimethyl orthoformateHCID 9005—
ReactantCodeinoneHCID 5459910—
SolventTolueneHCID 1140—
ProductThebaineHCID 5324289—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a dried 4-neck 5-liter round bottom flask equipped with a mechanical stirrer, heating mantle, pressure equalizing dropping funnel, and reflux condenser under a nitrogen atmosphere were added 100 g of codeinone, 500 mL of methanol and 73.5 mL of trimethyl orthoformate. The resulting mixture was allowed to stir at a temperature of from about 10° to about 15° C. Methanesulfonic acid (42 g) was then added to the flask at a temperature of about 10° C. to about 20° C. over a time period of about 10 minutes. To the resultant solution was added 500 mL of toluene, and the resulting mixture was allowed to reflux for about 3 h at a temperature of about 62° C. to about 64° C. until at least 93% of the codeinone was consumed. The reflux condenser was replaced with a distillation apparatus, the mixture was heated at a temperature of from about 91° C. to about 93° C., and methanol was allowed to distill from the reaction mixture until substantially all the methanol was removed. At various intervals an aliquot of the reaction mixture was removed, quenched in a phosphate buffer solution having a pH value of about 8, and analyzed using HPLC. The reaction mixture was monitored hourly until HPLC analysis showed that the peak corresponding to thebaine was at least about 95 percent of the total peak area (about 3 to 4 h). Dimethylformamide (22.4 mL) was then added to the reaction mixture, and the reaction mixture was heated at a temperature of from about 90° C. to about 95° C. for from about 3 to about 4 h. The mixture was cooled to about 25° C., deionized distilled water (500 mL) was added, and the resultant biphasic mixture was stirred at 25° C. for 0.5 h. The aqueous phase was collected, and to it was added iso-propanol (166 mL). The resultant mixture was heated to reflux, and treated with 25% NaOH (120 mL). The resultant slurry was slowly cooled with stirring to about 25° C. then further cooled to 0° C. to 5° C. and filtered. The solid was then washed with 3×50 mL of 3:1 (v:v) deionized distilled water:iso-propanol and dried under reduced pressure (40 mm Hg) at a temperature of from about 45° to about 50° C. for about 16 h to provide dry thebaine (67–80 g) as an off-white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06958398B1
Source datasetuspto-grants-2005_10
ORD IDord-62cce3c259cd4239b3f10e3b5e10e232
Source noteuspto-grants-2005_10