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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361639Generated: October 29, 2026

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

https://huagongshe.com/reaction/361639

Reaction equation

Participants

RoleNameHCIDCharge
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, extracted three times with ethyl acetate, 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 oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866560
Source datasetuspto-grants-1999_02
ORD IDord-69a8977141504ea1bf7407da1b9702bf
Source noteuspto-grants-1999_02