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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1708905Generated: October 26, 2026

Methyl iodide → 3Oxo-17beta-(hydroxymethyl)-4-methyl-4-androstene

https://huagongshe.com/reaction/1708905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant17beta-Hydroxymethyl-4-androsten-3-onHCID 14377617—
ReactantPotassium tert-butoxideHCID 23665647—
Solventtert-ButanolHCID 6386—
Product3Oxo-17beta-(hydroxymethyl)-4-methyl-4-androsteneHCID 67830249—

Reaction Steps

A mixture of potassium-t-butoxide (5 g) in 100 ml t-butanol is heated to reflux. A solution of 3-oxo-17β-(hydroxymethyl)-4-androstene (10 g) in t-butanol is added followed by a solution of methyl iodide (2.7 g) in t-butanol. Heating is continued for 3 hours. The mixture is then cooled, acidified, and extracted with dichloromethane. The dichloromethane solution is washed with brine, dried, and concentrated to yield 3oxo-17β-(hydroxymethyl)-4-methyl-4-androstene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04946834
Source datasetuspto-grants-1990_08
ORD IDord-daeaf2b01f0647c3a66a8a319af672d9
Source noteuspto-grants-1990_08