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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2051223Generated: November 1, 2026

Oxalyl chloride → HCID 53749054, compound

https://huagongshe.com/reaction/2051223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67926897HCID 67926897—
SolventTolueneHCID 1140—
ProductHCID 53749054HCID 53749054—

Reaction Steps

3-Carbomethoxy-3-androstene-17β-carboxylic acid, (360 mg, 0.78 mmol) was suspended in 10 ml of dry toluene and treated with 0.4 ml of oxalyl chloride for 2 hours under argon. The reaction mixture was then evaporated (1 mm Hg) and the residue was dissolved in 10 ml dry THF. A solution of 0.6 ml diisopropylamine in 2 ml dry THF was added and the reaction mixture stirred for 1 hour. The mixture was diluted with ice water and extracted with dichlorome thane. The organic layer was then washed twice with cold 5% hydrochloric acid, sodium hydroxide and brine; dried over sodium sulfate and evaporated. Chromatography on silica gel eluting with 20% ethyl acetate in hexane followed by recrystallization from diethyl ether afforded 3-carbomethoxy-3-androstene 178 N,N -diisopropylcarboxamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05017568
Source datasetuspto-grants-1991_05
ORD IDord-97e1ed1a60b64e04bde80fd6be91e67f
Source noteuspto-grants-1991_05