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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1973736Generated: November 1, 2026

Ammonium Chloride → 21-Ethyl-3alpha-hydroxy-5alpha-pregnane-11,20-dione

https://huagongshe.com/reaction/1973736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 86734286HCID 86734286—
ReactantHCID 178418348HCID 178418348—
SolventDiethyl EtherHCID 3283—
Product21-Ethyl-3alpha-hydroxy-5alpha-pregnane-11,20-dioneHCID 86734308—

Reaction Steps

Methyl lithium in ether (≈1.3M: 7.5 ml) was added slowly to a slurry of cuprous iodide (950 mg) in dry ether (40 ml) under nitrogen at -20°, the initial yellow precipitate just redissolving. 3α-Hydroxy-21-methylene-5α-pregnane-11,20-dione (500 mg) in dry ether (10 ml) was added rapidly to the solution forming a yellow precipitate. After 3/4 hr. at ≈0° the mixture was poured into saturated ammonium chloride solution and the oily precipitate extracted with ether. The extracts were washed with saturated ammonium chloride solution, then water, and dried over anhydrous sodium sulphate. The dried solution was evaporated to an off white foam (430 mg) which was purified by preparative t.l.c. in ethyl acetate/petrol (1:1). The main band (Rf ≈ 0.4) gave a white foam which on trituration with petrol, containing a small quantity of ether, gave title compound (320 mg.) as a white solid, m.p. 112°-113°, [α]D + 105° (c = 1.01).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03998829
Source datasetuspto-grants-1976_12
ORD IDord-20f8fc7da8544dd79437e9ea1e31f9b6
Source noteuspto-grants-1976_12