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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2231994Generated: October 31, 2026

Methanol → Osaterone

https://huagongshe.com/reaction/2231994

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantTetrahydrofuranHCID 8028—
ReactantOsaterone acetateHCID 114992—
ReactantSodium MethoxideHCID 10942334—
SolventWaterHCID 962—
ProductOsateroneHCID 3047806—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of 116 mg iof 17α-acetoxy-6-chloro-2-oxapregna-4,6-diene-3,20-dione, 0.5 ml of an about 28% methanol solution of sodium methylate, 0.1 ml of tetrahydrofuran and 5 ml of methanol was heated at 70° C. for 10 minutes. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed with a 30% aqueous solution of hydrogen chloride and then with a saturated aqueous solution of sodium hydrogen carbonate, and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the crude product was purified by TLC [developing solvent: chloroform/acetone (19/1)] to give 70 mg of 6-chloro-17α-hydroxy-2-oxapregna-4,6-diene-3,20-dione.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04785103
Source datasetuspto-grants-1988_11
ORD IDord-9ecddbe23f4349dda0d1aa4955ab27b2
Source noteuspto-grants-1988_11