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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 11beta-Trimethylsiloxy-21-acetoxy-6alpha-fluoropregna-1,4,16-triene-3,20-dione | HCID 22798531 | — |
| Reactant | HCID 178477771 | HCID 178477771 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 11beta-Trimethylsiloxy-21-acetoxy-6alpha-fluoro-16alpha-methyl-pregna-1,4-diene-3,20-dione | HCID 22798530 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04036831 |
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| Source dataset | uspto-grants-1977_07 |
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| ORD ID | ord-2f0fec28d7ee463c898190a6631089de |
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| Source note | uspto-grants-1977_07 |
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