Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1952785Generated: October 26, 2026

Oxalyl chloride → 3-Oxoandrost-4-ene-17beta-carbonyl chloride

https://huagongshe.com/reaction/1952785

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant(17beta)-3-Oxoandrost-4-ene-17-carboxylic acidHCID 99472—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product3-Oxoandrost-4-ene-17beta-carbonyl chlorideHCID 11727386—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a stirred solution of 3-oxoandrost-4-ene-17β-carboxylic acid (30 g) in methylene chloride (300 mL) and dimethylformamide (1.82 mL) a solution of oxalyl chloride (9.28 mL) in methylene chloride (30 mL) was added dropwise at 0° C. under nitrogen atmosphere. After stirring at 0° C. for 1 hour the reaction was completed. The volatile compounds were removed under vacuum, the solid was taken up with cyclohexane (200 mL) and evaporated to dryness (twice). The 3-oxo-androst-4-ene-17β-carbonyl chloride (30.33 g) so obtained was dissolved in chloroform (1.5 L), cooled to 0° C. and treated with 1,1,1,3,3,3-hexafluorophenylpropyl amine (46.078 g) and pyridine (38.3 mL). The reaction mixture was heated at reflux for 7 hours. After staying overnight at room temperature the reaction mixture was washed with 1N HCl (2×100 mL), with brine, with water until neutral and dried over sodium sulfate. The solvent was evaporated under vacuum and the brownish solid purified by flash chromatography on silica gel (eluant: n-hexane/ethyl acetate 70/30) to yield 9.2 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06114345
Source datasetuspto-grants-2000_09
ORD IDord-a3960a24873d48539f37896ca9c6946c
Source noteuspto-grants-2000_09