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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1701444Generated: October 26, 2026

Sodium borohydride → Methyl 3alpha,11beta-dihydroxy-5alpha-androstane-17beta-carboxylate

https://huagongshe.com/reaction/1701444

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant3alpha-Hydroxy-17beta-methoxycarbonyl-5alpha-androstan-11-oneHCID 70586102—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductMethyl 3alpha,11beta-dihydroxy-5alpha-androstane-17beta-carboxylateHCID 7058399864%

Reaction Steps

Sodium borohydride (1.24 g) in water (7 ml) was added to a solution of methyl 3α-hydroxy-11-oxo-5α-androstane-17β-carboxylate (2.58 g) in methanol (60 ml) and the mixture refluxed for 30 minutes. A further portion of sodium borohydride (200 mg) in a little water was added and refluxing continued for 10 minutes more. Most of the solvent was removed in vacuo and, after cooling, the crystalline product was collected by filtration. Recrystallization from aqueous methanol afforded title compound (1.662 g),

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04192871
Source datasetuspto-grants-1980_03
ORD IDord-6376352dd74d4b18802333614636161f
Source noteuspto-grants-1980_03