HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 918372Generated: October 30, 2026
2-Methyl-3-diazo-1-propene → 21-Chloro-9-fluoro-11beta,17-dihydroxy-16alpha-((2-methyl-2-propenyl)oxy)pregna-1,4,diene-3,20-dione
https://huagongshe.com/reaction/918372
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Methyl-3-diazo-1-propene | HCID 21520845 | — |
| Reactant | 21-Chloro-9-fluoro-11beta,16alpha,17-trihydroxypregna-1,4-diene-3,20-dione | HCID 86733740 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 21-Chloro-9-fluoro-11beta,17-dihydroxy-16alpha-((2-methyl-2-propenyl)oxy)pregna-1,4,diene-3,20-dione | HCID 86733739 | — |
Reaction Steps
A solution of 2-methyl-3-diazo-1-propene in 150 ml of ether (prepared from 0.1 mole of N-(2-methyl-2-propenyl)-ethyl carbamate by the method of J. L. Brewbaker and H. Hart, J. Am. Chem., Soc., 91, 711 (1969)) is diluted with 50 ml of methanol and cooled to 0°C. A total of 7 g of 21-chloro-9-fluoro-11β,16α,17-trihydroxypregna-1,4diene-3,20-dione, 16,17-cycloborate is added in portions until nitrogen evolution ceases. The solvent is removed in vacuo and the residue is dissolved in chloroform and chromatographed on an 80 g -silica gel column. Elution with chloroform gives TLC pure material which crystallizes from acetone-hexane to give 5.4 g of 21-chloro-9-fluoro-11β,17 -dihydroxy-16α-[(2-methyl-2-propenyl)oxy]pregna-1,4-diene-3,20-dione, melting point 238°-240°C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US03971772 |
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| Source dataset | uspto-grants-1976_07 |
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| ORD ID | ord-6d668e3188bc41deb95a1ddd13988844 |
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| Source note | uspto-grants-1976_07 |
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