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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 259155Generated: October 25, 2026

Ammonium Chloride → 11beta-Trimethylsiloxy-21-acetoxy-6alpha-fluoro-16alpha-methyl-pregna-1,4-diene-3,20-dione

https://huagongshe.com/reaction/259155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
Reactant11beta-Trimethylsiloxy-21-acetoxy-6alpha-fluoropregna-1,4,16-triene-3,20-dioneHCID 22798531—
ReactantHCID 178477771HCID 178477771—
SolventDichloromethaneHCID 6344—
Product11beta-Trimethylsiloxy-21-acetoxy-6alpha-fluoro-16alpha-methyl-pregna-1,4-diene-3,20-dioneHCID 22798530—

Reaction Conditions

Temperature-10 °C

Reaction Steps

750 mg cuprous iodide was suspended in 10 ml dichloromethane in an atmosphere of nitrogen and cooled to -10° C. To this suspension under stirring and cooling was added 9 ml of a 2% solution of lithium-methyl by drop wise addition maintaining the temperature below -5°. To the so obtained lithium-dimethyl-copper solution was added 425 mg 11β-trimethylsiloxy-21-acetoxy-6α-fluoropregna-1,4,16-triene-3,20-dione obtained according to Example 8 dissolved in 3 ml dichloromethane. The temperature of the reaction mixture was kept below -1°, and the stirring was maintained for a period of 15 minutes. The reaction mixture was poured into an aqueous ammonium chloride solution, the organic phase separated and the aqueous phase re-extracted with dichloromethane. The organic extracts were combined, washed with water, dried over anhydrous sodium sulfate and concentrated to dryness under reduced pressure. Trituration with acetone afforded a crystalline product 11β-trimethylsiloxy-21-acetoxy-6α-fluoro-16α-methyl-pregna-1,4-diene-3,20-dione (compound 14) yield 320 mg TLC: homogeneous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04036831
Source datasetuspto-grants-1977_07
ORD IDord-2f0fec28d7ee463c898190a6631089de
Source noteuspto-grants-1977_07