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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1603324Generated: November 2, 2026

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

https://huagongshe.com/reaction/1603324

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 numberUS05986115
Source datasetuspto-grants-1999_11
ORD IDord-e12368985fa646b9a6de475a5e399993
Source noteuspto-grants-1999_11