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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196317Generated: November 1, 2026

Pyridine → 6alpha,7alpha-Diepoxypregn-4-en-3beta-yl acetate

https://huagongshe.com/reaction/1196317

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
Reactant6alpha,7alpha-Diepoxypregn-4-en-3beta-olHCID 86745799—
SolventDichloromethaneHCID 6344—
Product6alpha,7alpha-Diepoxypregn-4-en-3beta-yl acetateHCID 8674580090%

Reaction Steps

To a mixture of 0.084 g (0.189 mmole) of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α;6α,7α-diepoxypregn-4-en-3β-ol, 0.5 ml (6.18 mmoles) of dry pyridine and 5 ml of methylene chloride was gradually added 0.1 ml (1.06 mmoles) of acetic anhydride dropwise at a temperature of 0° C. and the solution was stirred at room temperature for 8 hours. The reaction mixture thus obtained was diluted with methylene chloride and washed with saturated aqueous copper (II) sulfate solution. The aqueous layer (washings) was extracted with methylene chloride and the extract was combined with the organic layer. The resulting mixture was washed with water and aqueous sodium chloride solution in that order and dired over magnesium sulfate. The solvent was then distilled off under reduced pressure and the residue was purified by silica gel chromatography (eluent: ethyl acetate-hexane: 1:10, v/v) to recover 0.083 g of 20-(5,5-dimethyl-1,3-dioxan-2-yl)-1α,2α;6α,7α-diepoxypregn-4-en-3β-yl acetate (yield: 90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112998
Source datasetuspto-grants-1992_05
ORD IDord-f5fcedadc12a445fb90b776e58929db0
Source noteuspto-grants-1992_05