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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 726135Generated: October 31, 2026

17beta-Carbomethoxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one → 17Hydroxymethyl-3-hydroxy-6-t-butoxycarbonyl-6-azaandrost-4-ene

https://huagongshe.com/reaction/726135

Reaction equation

Participants

RoleNameHCIDCharge
Reactant17beta-Carbomethoxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-oneHCID 10002872—
ReactantDiisobutylaluminumhydrideHCID 21225700—
SolventDichloromethaneHCID 6344—
Product17Hydroxymethyl-3-hydroxy-6-t-butoxycarbonyl-6-azaandrost-4-eneHCID 22881208—

Reaction Steps

A solution of 17β-carbomethoxy-6-t-butoxycarbonyl-6-azaandrost-4-en-3-one (2.30 g, 5.33 mmol), example 1, part E, in methylene chloride (70 mL) at -78° C. is treated with diisobutylaluminum hydride (1.5M in toluene, 15 mL, 22.5 mmol). After 20 minutes the reaction is quenched with methanol (4 mL), methylene chloride added (150 mL), washed with 2N NaOH and water, dried over MgSO4 and concentrated to give crude 17hydroxymethyl-3-hydroxy-6-t-butoxycarbonyl-6-azaandrost-4-ene of sufficient purity to carry on to the following steps; yield: 2.16 g (99%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05708001
Source datasetuspto-grants-1998_01
ORD IDord-6c66fbcbf77e44e28af67cf917a3ccce
Source noteuspto-grants-1998_01