HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 279829Generated: November 1, 2026
Ammonium Chloride → HCID 13131725, compound
https://huagongshe.com/reaction/279829
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 70470448 | HCID 70470448 | — |
| Reactant | HCID 178418348 | HCID 178418348 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 13131725 | HCID 13131725 | 125.5% |
Reaction Steps
Under argon at 0° C., 200 ml of a 5% solution of methyllithium in ether is added dropwise to a suspension of 36.5 g of copper(I) iodide in 730 ml of anhydrous tetrahydrofuran. The yellow solution is cooled to -30° C., and a solution of 29.0 g of 11β,17-dihydroxy-21-isovaleryloxy-6α-methyl-1,4-pregnadiene-3,20-dione in 730 ml of anhydrous tetrahydrofuran is added thereto. The mixture is stirred further for 10 minutes at -25° C. and poured onto an aqueous ammonium chloride solution. After extraction with methylene chloride, the organic solution is washed, dried over sodium sulfate, and evaporated under vacuum. The crude product is purified on 750 g of silica gel with a methylene chloride-acetone gradient (0-20% acetone), yielding 18.2 g of 11β,21-dihydroxy-17-isovaleryloxy-6α-methyl-1,4-pregnadiene-3,20-dione, mp 164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04587236 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-032beb7b537541ada97552650239afea |
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| Source note | uspto-grants-1986_05 |
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