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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267634Generated: October 31, 2026

Ethanol → 2beta-Ethoxy-3alpha-hydroxy-5alpha-androstan-11-one-17beta-carboxylic acid

https://huagongshe.com/reaction/267634

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantWaterHCID 962—
ReactantSulfuric AcidHCID 1118—
ReactantHCID 22788254HCID 22788254—
Product2beta-Ethoxy-3alpha-hydroxy-5alpha-androstan-11-one-17beta-carboxylic acidHCID 22788255—

Reaction Steps

A solution of 2α,3α-epoxy-5α-androstan-11-one-17β-carboxylic acid (940 mg.) and concentrated sulphuric acid (0.25 ml.) in dry ethanol (30 ml.) was stirred at room temperature for 30 minutes. Water (100 ml.) was added and the reaction mixture extracted with chloroform. The chloroform solution was washed with water, dried, filtered and evaporated to give a froth which solidified when triturated with chloroform/petrol. Filtration afforded the solid crude product (752 mg.) which, after recrystallisation from ethanol/water, afforded the pure title compound; m.p. 249°-260°; [α]D + 74°, (c 0.33).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03943124
Source datasetuspto-grants-1976_03
ORD IDord-3dc92c77d11c46c3acca2060d857e6e2
Source noteuspto-grants-1976_03