HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1577862Generated: November 1, 2026
Perchloric Acid → 21-Acetoxy-6alpha-chloro-9,11beta-epoxy-16alpha-methyl-9beta-pregna-1,4-diene-3,20-dione
https://huagongshe.com/reaction/1577862
Participants
| Role | Name | HCID | Charge |
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| Reactant | Perchloric Acid | HCID 24247 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 21-Acetoxy-6alpha-chloro-16alpha-methyl-1,4,9(11)-pregnatriene-3,20-dione | HCID 22817430 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 21-Acetoxy-6alpha-chloro-9,11beta-epoxy-16alpha-methyl-9beta-pregna-1,4-diene-3,20-dione | HCID 86738014 | 41.7% |
Reaction Steps
A solution of 12.0 g of 21-acetoxy-6α-chloro-16α-methyl-1,4,9(11)-pregnatriene-3,20-dione in 120 ml of dioxane is stirred at room temperature after adding 11.1 g of N-bromosuccinimide and 60 ml of 10% perchloric acid and, after 60 minutes, poured into ice water. The thus-precipitated product is filtered off, washed with water, dried in the air, and dissovled in 215 ml of ethanol. After adding 29 g of potassium acetate, the solution is heated for 8 hours to 60° C. under argon. Then the mixture is concentrated to a volume of 60 ml under vacuum, and stirred into ice water. The precipitated product is isolated and chromatographed on silica gel. With 8-9% acetone-hexane, after recrystallization from acetone-diisopropyl ether, 5.2 g of 21-acetoxy-6α-chloro-9,11β-epoxy-16α-methyl-9β-pregna-1,4-diene-3,20-dione is obtained, m.p. 189° C. [α]D25 =+57° (chloroform).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04289763 |
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| Source dataset | uspto-grants-1981_09 |
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| ORD ID | ord-6076137a15894860bb94e0de0eb4cc8b |
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| Source note | uspto-grants-1981_09 |
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