Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900678Generated: October 30, 2026

Trimethyl orthoformate → 3-Ethylenedioxy-11beta-fluoro-7alpha-methylestr-5(10)-en-17beta-ol

https://huagongshe.com/reaction/900678

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethyl orthoformateHCID 9005—
ReactantSodium CarbonateHCID 10340—
Reactantp-Toluenesulfonic acid monohydrateHCID 521998—
Reactant11beta-Fluoro-17beta-hydroxy-7alpha-methylestr-4-en-3-oneHCID 9904638—
SolventEthylene GlycolHCID 174—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product3-Ethylenedioxy-11beta-fluoro-7alpha-methylestr-5(10)-en-17beta-olHCID 86597450—

Reaction Steps

3.63 ml of ethylene glycol and 1.82 ml of trimethyl orthoformate and 23.6 ml of para-toluenesulfonic acid hydrate were added to a solution of 500 mg of 11β-fluoro-17β-hydroxy-7α-methyl-estr-4-en-3-one (I) in 6.35 ml of dichloromethane. The reaction mixture was stirred for 20 hours at room temperature. Then, it was mixed with sodium carbonate solution, diluted with ethyl acetate, washed neutral, dried on sodium sulfate, concentrated by evaporation in a vacuum and chromatographed on silica gel with hexane/ethyl acetate. 170 mg of 3-ethylenedioxy-11β-fluoro-7α-methylestr-5(10)-en-17β-ol (C), which contained portions of double-bond-isomeric 3-ethylenedioxy-11β-fluoro-7α-methylestr-5-en-17β-ol (C), was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361645B2
Source datasetuspto-grants-2008_04
ORD IDord-855d177f12974593abd7ebbbd9a30865
Source noteuspto-grants-2008_04