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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595967Generated: November 1, 2026

Water → 7alpha-(5-Acetoxypentyl)-3-hydroxy-estra-1,3,5(10)-trien-17-one

https://huagongshe.com/reaction/1595967

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantLithium BromideHCID 82050—
ReactantHCID 15838157HCID 15838157—
CatalystCopper bromide (CuBr2)HCID 24611—
SolventAcetonitrileHCID 6342—
Product7alpha-(5-Acetoxypentyl)-3-hydroxy-estra-1,3,5(10)-trien-17-oneHCID 1583815873.8%

Reaction Steps

17.8 g of lithium bromide and 92.83 g of copper(II) bromide are added to a solution of 82.3 g of 7α-(5-acetoxypentyl)-estr-4-ene-3,17-dione in 936 ml of acetonitrile at a bath temperature of 80° C. After 10 minutes at a bath temperature of 80° C., the reaction solution is cooled, mixed with water, extracted three times with ethyl acetate, the organic phase is washed with water and sodium bicarbonate solution and dried. The residue that is obtained after the concentration by evaporation is chromatographed on silica gel, and 60.4 g of 7α-(5-acetoxypentyl)-3-hydroxy-estra-1,3,5(10)-trien-17-one is obtained as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288051B1
Source datasetuspto-grants-2001_09
ORD IDord-f78c164df42b4672803353e2077ea925
Source noteuspto-grants-2001_09