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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2108334Generated: October 30, 2026

Acetic Anhydride → HCID 9929412, compound

https://huagongshe.com/reaction/2108334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 57629370HCID 57629370—
SolventPyridineHCID 1049—
ProductHCID 9929412HCID 9929412—

Reaction Steps

A mixture of crude 17,17-ethylenedioxyandrosta-1.5-dien-3β-ol (4, 1.2 g) in pyridine (10 ml) and acetic anhydride (3 ml) was stirred at room temperature for 16 hours. The reaction mixture was poured into ice-water and the compound was extracted with ether. The organic layer was washed with ice-water several times followed by brine and dried over anhydrous magnesium sulfate. Evaporation of the solvent in vacuo below 35° C. gave 1.0 g of crude solid. Recrystallization from methanol gave 3β-acetoxy-17,17-ethylenedioxyandrosta-1,5-diene (5). Mp. 105-6° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07514420B2
Source datasetuspto-grants-2009_04
ORD IDord-c35149602ede4a0ca33686c35f7191ca
Source noteuspto-grants-2009_04