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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1089426Generated: November 4, 2026

Pyridine → HCID 15085902, compound

https://huagongshe.com/reaction/1089426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 15085897HCID 15085897—
ReactantHCID 15085901HCID 15085901—
SolventWaterHCID 962—
ProductHCID 15085902HCID 15085902—
ProductHCID 15085903HCID 15085903—

Reaction Steps

4,4-Difluoro-17β-(cyclopropyloxy)androst-5-en-3β-ol is treated with acetic anhydride and pyridine. The mixture is poured into water and extracted with ethyl acetate. The ethyl acetate layer is separated and dried and the solvent is evaporated to leave as a residue, 3β-acetyloxy-4,4-difluoro-17β-(cyclopropyloxy)androst-5-ene. 3β-(Cyclopentanepropionyloxy)-4,4-difluoro-17β-(cyclopropyloxy)androst-5-ene and 3β-(benzenepropionyloxy)-4,4-difluoro-17β-(cyclopropyloxy)androst-5-ene are obtained in a similar way using the appropriate acid chlorides.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04966897
Source datasetuspto-grants-1990_10
ORD IDord-a81193e0660c44fc8e0a23bacc2bfbc7
Source noteuspto-grants-1990_10