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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267615Generated: November 2, 2026

Sodium borohydride → HCID 86733133, compound

https://huagongshe.com/reaction/267615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86733134HCID 86733134—
SolventMethanolHCID 887—
ProductHCID 86733133HCID 8673313318%

Reaction Steps

17β-Methoxycarbonylandrost-4-ene-3,11-dione (2.8 g.) was dissolved in dry methanol (250 ml.) and to the stirred solution was added sodium borohydride (600 mg.) in portions over 2 hours. The reaction was then left to stand for 30 minutes, and then concentrated by evaporation under reduced pressure and poured on to ice. The precipitate was extracted into chloroform and the organic solution was dried over sodium sulphate and evaporated to an oil which was purified by preparative TLC to give 3β-hydroxy-17β-methoxycarbonylandrost-4-en-11-one (506 mg.) as colourles plates, m.p. 197°-201°, [α]D 30 144°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03943124
Source datasetuspto-grants-1976_03
ORD IDord-1c7ef05873e048bd9c9b665b8ce326f8
Source noteuspto-grants-1976_03