Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430706Generated: October 30, 2026

Hydrochloric Acid → 17-Allyl-3,14beta-dihydroxy-4,5alpha-epoxy-6beta-methylaminomorphinan

https://huagongshe.com/reaction/430706

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantNaloxone HydrochlorideHCID 5464092—
ReactantMethylamine hydrochlorideHCID 6364545—
SolventMethanolHCID 887—
Product17-Allyl-3,14beta-dihydroxy-4,5alpha-epoxy-6beta-methylaminomorphinanHCID 5424824224%
Product17-Allyl-3,14beta-dihydroxy-4,5alpha-epoxy-6alpha-methylaminomorphinanHCID 5424824312%

Reaction Steps

Naloxone hydrochloride (3.0 g), methylamine hydrochloride (5.57 g) and sodium cyanoborohydride (0.33 g) were suspended in anhydrous methanol (40 ml) and stirred for 17 hours at room temperature. After addition of concentrated hydrochloric acid (1.0 ml) and removal of solvent by distillation, distilled water (50 ml) was added followed by washing with chloroform (20 ml). Saturated aqueous sodium bicarbonate (10 ml) was added to make the solution basic followed by extraction with chloroform (30 ml×3). After drying with anhydrous magnesium sulfate, the solvent was distilled off. The resulting crude product was purified with silica gel column chromatography (Merk 7734 100 g; ethyl acetate/methanol/aqueous ammonia=90/10/1->80/20/2) to obtain the target compound in the form of a pure fraction (12 0.4 g, 12%; 13 0.8 g, 24%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06323212B1
Source datasetuspto-grants-2001_11
ORD IDord-497a86575f1a4d57a396c41a34163baf
Source noteuspto-grants-2001_11