Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | 3-Hydroxypregna-5,16-dien-20-one 3-acetate | HCID 10904398 | — |
| Reactant | Trimethylaluminum | HCID 16682925 | — |
| Catalyst | copper(I) bromide | HCID 24593 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | HCID 67557649 | HCID 67557649 | — |
Reaction Steps
3.56 g (10 mmol) of 3-acetoxy-pregna-5,16-dien-20-one is dissolved in 20 ml of dioxane at 20° C. and mixed with 143.3 g (1 mmol) of copper(I) bromide. 11 ml (11 mmol) of a 1 molar solution of trimethyl aluminum in hexane is added to the reaction at room temperature under nitrogen atmosphere and, after completion of the addition, stirred for 3 hours more at 22° C. For hydrolysis of the reaction solution, 1 ml of water dissolved in 5 ml of dioxane is carefully added to the reaction. It is stirred for 10 minutes more and the inorganic precipitate is filtered off with dioxane and washed again. The dioxane solution is concentrated by evaporation on a rotary evaporator and the residue is chromatographed on silica gel with ethyl acetate/hexane as eluent. After concentration by evaporation of the fractions, 1.72 g of 3-acetoxy-16α-ethyl-pregn-5-en-20-one (45% of theory) of a melting point of 114.9° C. is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05908944 |
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| Source dataset | uspto-grants-1999_06 |
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| ORD ID | ord-8bed8918a56743c38e11d471ec4cb389 |
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| Source note | uspto-grants-1999_06 |
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