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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64724Generated: October 25, 2026

N,N-Dimethylaniline → 16beta-Ethyl-17beta-(2-methylvaleryl)oxyacetoxy-4-estren-3-one

https://huagongshe.com/reaction/64724

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN,N-DimethylanilineHCID 949—
Reactant2-Methylvaleryl chlorideHCID 107385—
Reactant16beta-Ethyl-17beta-glycoloyloxy-4-estren-3-oneHCID 70466441—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product16beta-Ethyl-17beta-(2-methylvaleryl)oxyacetoxy-4-estren-3-oneHCID 7046693019.8%

Reaction Steps

In 20 ml of dichloromethane are dissolved 0.5 g of 16β-ethyl-17β-glycoloyloxy-4-estren-3-one and 0.2 ml of N,N-dimethylaniline, and 0.5 g of 2-methylvaleryl chloride is added to the above solution. The mixture is refluxed for 6 hours. After cooling, the reaction mixture is diluted with 150 ml of ethyl acetate and dried over anhydrous magnesium sulfate. The solvent is then distilled off under reduced pressure and the residue is subjected to column chromatography. Following passage of 200 ml of diisopropyl ether-n-hexane (2:8), elution is carried out with 500 ml of a 1:1 mixture of the same solvents. The eluate is evaporated under reduced pressure to remove the solvent, giving 0.126 g of the above-identified compound as a light-yellow viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04609650
Source datasetuspto-grants-1986_09
ORD IDord-6c373de8ad0a482ca08749a90e9f07a1
Source noteuspto-grants-1986_09