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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051221Generated: October 30, 2026

Imidazole → 3-Oxo-17beta-(t-butyldimethylsilyloxymethyl)-4-androstene

https://huagongshe.com/reaction/2051221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant17beta-Hydroxymethyl-4-androsten-3-onHCID 14377617—
SolventDimethylformamideHCID 6228—
Product3-Oxo-17beta-(t-butyldimethylsilyloxymethyl)-4-androsteneHCID 1480133082%

Reaction Steps

To a solution of 3-oxo-17β-(hydroxymethyl) 4 androstene (15 g, 0.05 mol) in 200 ml DMF was added 5.8 g (0.085 mol) imidazole followed by 9.7 g (0.065 mol) t-butyldimethylsilyl chloride. The reaction mixture was stirred at room temperature under argon, for 2.5 hours. The reaction mixture was then poured into 250 ml ice water and washed 3 times with ethyl acetate. The combined organic layers were washed twice with cold 5% hydrochloric acid and once each with saturated sodium bicarbonate solution and brine. The organic layer was dried over sodium sulfate and evaporated. Recrystallization from methanol afforded 16.9 g (82%) of 3-oxo-17β-(t-butyldimethylsilyloxymethyl) -4-androstene as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017568
Source datasetuspto-grants-1991_05
ORD IDord-4055809880684a1bbd780d7c1baf3c5f
Source noteuspto-grants-1991_05