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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2370711Generated: October 27, 2026

Methanesulfonyl chloride → Naltrexone Base

https://huagongshe.com/reaction/2370711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantCyclopropanemethanolHCID 75644—
ReactantLithium BromideHCID 82050—
Reactant(-)-NoroxymorphoneHCID 5497189—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductNaltrexone BaseHCID 21159611—

Reaction Conditions

Temperature2.5 °C

Reaction Steps

Methanesulphonyl chloride (76 kg) was added to the mixture of cyclopropyl methanol (50 kg) and triethylamine (192 L) in DMF (400 L) maintained at 0-5° C., the reaction mixture was maintained at 0-5° C. for 3.0 hrs. Lithium bromide (60 Kg) was added to reaction mixture at 0-15° C. and maintained for 10-15 minutes. Noroxymorphone (40 Kg) was added to above reaction mixture at 0-5° C. and temperature raised to 65-70° C. over 1.0 hr period and maintained for 14-15 hrs. After completion of reaction it was quenched in ice-water below 20° C. and the product was extracted with ethylacetate, The ethylacetate layer was concentrated and the product was isolated with MDC and cyclohexane mixture at 10-15° C. Yield=35.3 Kg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08710226B2
Source datasetuspto-grants-2014_04
ORD IDord-bafd9c47a089478abd0cff8ba67ed933
Source noteuspto-grants-2014_04