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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1455879Generated: October 31, 2026

Dehydroepiandrosterone → 1476-64-8

https://huagongshe.com/reaction/1455879

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDehydroepiandrosteroneHCID 5881—
ReactantDichloromethaneHCID 6344—
ReactantSodium AcetateHCID 517045—
ReactantEthyl cysteinate hydrochlorideHCID 2723617—
SolventEthanolHCID 702—
Product1476-64-8HCID 7056608—

Reaction Steps

Following the procedure described by Djerassi (C. Djerassi, N. Crossley and M. A. Kielczewski, J. Org. Chem. 27, 1112, 1962), dehydroepiandrosterone (2.88 g, 10 mmol) is dissolved in anhydrous ethanol, sodium acetate is added followed by L-cysteine ethyl ester hydrochloride (18 g, 100 mmol) and the mixture is heated overnight under an argon atmosphere. The reaction mixture is then evaported under vacuum. Methylene chloride is added to precipitate excess of L-cysteine ethyl ester hydrochloride. The solution is then filtered and the filtrate is washed twice with water, dried on magnesium sulfate, filtered and evaporated under vacuum. The residue is triturated with ethanol to give crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05843932
Source datasetuspto-grants-1998_12
ORD IDord-4c3b043ddada4e83a3e74a2a5003221f
Source noteuspto-grants-1998_12