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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 361664Generated: October 30, 2026

Benzyl Bromide → 3-Benzyloxy-7alpha-(5-hydroxypentyl)-estra-1,3,5(10),15-tetra-en-17-one

https://huagongshe.com/reaction/361664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl BromideHCID 7498—
ReactantCesium carbonateHCID 10796—
Reactant3-Hydroxy-7alpha-(5-hydroxypentyl)-estra-1,3,5(10),15-tetraen-17-oneHCID 15838163—
SolventAcetoneHCID 180—
Product3-Benzyloxy-7alpha-(5-hydroxypentyl)-estra-1,3,5(10),15-tetra-en-17-oneHCID 57272166—

Reaction Steps

A solution of 2.85 g of 3-hydroxy-7α-(5-hydroxypentyl)-estra-1,3,5(10),15-tetraen-17-one in 57 ml of acetone is mixed with 3.25 g of cesium carbonate and 1.14 ml of benzyl bromide, and the mixture is refluxed for 1 hour. The reaction mixture is concentrated by evaporation, the residue is mixed with water, shaken out with ethyl acetate, the organic phase is dried on sodium sulfate and concentrated by evaporation. The residue is chromatographed on silica gel with hexane/ethyl acetate. 3.12 g of 3-benzyloxy-7α-(5-hydroxypentyl)-estra-1,3,5(10),15-tetraen-17-one is obtained as foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05866560
Source datasetuspto-grants-1999_02
ORD IDord-e50b2b66eee14950bbc54d54b4b7f168
Source noteuspto-grants-1999_02