Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2254633Generated: October 31, 2026

Potassium sodium tartarate → 17beta-Acetoxy-17alpha-methyl-3-oxoandrost-4-ene-7alpha-carbonitrile

https://huagongshe.com/reaction/2254633

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium sodium tartarateHCID 9855836—
Reactant17beta-Acetoxy-17alpha-methylandrosta-4,6-dien-3-oneHCID 12832214—
ReactantDiethyl aluminum cyanideHCID 16686413—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product17beta-Acetoxy-17alpha-methyl-3-oxoandrost-4-ene-7alpha-carbonitrileHCID 6778118670.5%

Reaction Steps

At room temperature, 17.1 g of 17β-acetoxy-17α-methylandrosta-4,6-dien-3-one [U.S. Pat. No. 3,033,752 (1962)] in 170 ml of toluene is combined with 100 ml of diethyl aluminum cyanide solution (1 mole in toluene). After 24 hours, the reaction mixture is introduced into a potassium sodium tartrate solution, diluted with ethyl acetate, and the mixture is stirred for 1 hour at room temperature, extracted with ethyl acetate, the organic phase is washed with water, dried, and concentrate under vacuum. The resultant crude product is allowed to react in 500 ml of methanol at room temperature with 360 mg of potassium carbonate, the mixture is concentrated under vacuum after 2.5 hours, diluted with ethyl acetate, washed with water, and dried. After the crude product has been chromatographed on silica gel with a methylene chloride (tert-butyl methyl ether) gradient, 13 g of 17β-acetoxy-17α-methyl-3-oxoandrost-4-ene-7α-carbonitrile is obtained, mp 211°-216° C. (from isopropyl ether).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05236912
Source datasetuspto-grants-1993_08
ORD IDord-627120541d38480e9ce86b108243e822
Source noteuspto-grants-1993_08