Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 23396842 | HCID 23396842 | — |
| Catalyst | Copper bromide (CuBr2) | HCID 24611 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 15513552 | HCID 15513552 | — |
Reaction Steps
43.55 g of 11β-fluoro-4-estren-17-ol-3-one (150 mmol, Tetrahedron Letters 1995, 2611) is suspended in 1500 ml of acetonitrile, 50 g of copper(II) bromide is added, and it is stirred at room temperature. After 16 hours, additional copper(II) bromide is added in three portions (25 g, 12 g, 6 g) within 6 hours, and finally stirred for another 6 hours at room temperature. The reaction mixture is cooled in an ice bath, mixed with 500 ml of water and extracted with ethyl acetate. The organic phase is mixed with a little methanol, washed with saturated bicarbonate solution and common salt solution and dried with sodium sulfate. After concentration by evaporation, the substance crystallizes out, yield 30.8 g (71% of theory), flash point 233-234° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06958327B1 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-7e1d6c0d46bf41239368e55912e886be |
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| Source note | uspto-grants-2005_10 |
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