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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1908982Generated: October 28, 2026

Acetic Acid → Nalmefene hydrochloride

https://huagongshe.com/reaction/1908982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
ReactantNaltrexoneHCID 5360515—
ReactantHCID 178418922HCID 178418922—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventWaterHCID 962—
Solvent2-MethyltetrahydrofuranHCID 7301—
ProductNalmefene hydrochlorideHCID 538888198.9%

Reaction Steps

Methyltriphenylphosphonium bromide (MTPPB, 112.9 g) was suspended in 2-methyltetrahydrofuran (MTHF, 245 ml). Keeping the temperature in the range 20-25° C., KO-t-Bu (38.7 g) was charged in portions under inert atmosphere in one hour. The suspension was stirred for two hours. An anhydrous solution of naltrexone (35 g) in MTHF (144 ml) was then added over a period of one hour at 20-25° C. The suspension was maintained under stirring overnight. The mixture was then treated with a solution of glacial acetic acid (17.7 g) in MTHF. Water was then added and the pH was adjusted to 9-10. The phases were separated, the lower aqueous phase was discarded and the organic phase was washed twice with water. The organic phase was concentrated to residue under vacuum and then diluted with dichloromethane (175 ml) to give a clear solution. Concentrated aqueous hydrochloric acid (HCl 37%, 10.1 g) was added over one hour at 20-25° C. The suspension was stirred and then filtered and washed with dichloromethane and acetone. The product was dried affording 38.1 g of Nalmefene HCl.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598352B2
Source datasetuspto-grants-2013_12
ORD IDord-8dc998d385814cf18ed793457598736e
Source noteuspto-grants-2013_12