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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613969Generated: October 26, 2026

Acetic Anhydride → 21-Acetoxy-3,3-ethylenedioxy-20-nitropregna-5,16-dien-9alpha-ol

https://huagongshe.com/reaction/1613969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant3,3-Ethylenedioxy-20-nitropregna-5,16-diene-9alpha,21-diolHCID 54277511—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product21-Acetoxy-3,3-ethylenedioxy-20-nitropregna-5,16-dien-9alpha-olHCID 57121005—

Reaction Steps

Acetic anhydride (1.5 ml) was added to a stirred suspension of 3,3-ethylenedioxy-20-nitropregna-5,16-diene-9α,21-diol (1.00 g of diastereomer II, prepared according to example 2), and 4-dimethylaminopyridine (100 mg) in methylene chloride (10 ml) to give a clear solution. The reaction mixture was stirred for an additional 30 minutes and concentrated under reduced pressure. The residue was dissolved in methylene chloride and filtered over a silica gel column. The filtrate was evaporated under reduced pressure to afford a white solid which was dried under reduced pressure at 50° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05194602
Source datasetuspto-grants-1993_03
ORD IDord-bfd665e02d7842369a83420e9194bc70
Source noteuspto-grants-1993_03