HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Bromoacetamide → 4beta-Bromo-24,24-difluoro-25-hydroxy-5beta-cholestan-3-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Bromoacetamide | HCID 4353 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 24,24-Difluoro-5beta-cholestane-3alpha,25-diol | HCID 70565201 | — |
| Solvent | Hydrogen Bromide | HCID 260 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 4beta-Bromo-24,24-difluoro-25-hydroxy-5beta-cholestan-3-one | HCID 70563380 | — |
Reaction Steps
To a solution of 800 mg of 24,24-difluoro-5β-cholestane-3α,25-diol (Va) in 32 ml of tert-butyl alcohol, 15 ml of water, 200 μl of 48% hydrobromic acid and 800 mg of N-bromoacetamide were added. After stirring at room temperature for 3 days, ethyl acetate was added to the reaction mixture, which was then washed sequentially with 0.5% aqueous sodium thiosulfate and saturated aqueous sodium chloride, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the resulting residue was purified through a short column (5 g of silica gel) to produce 950 mg of a crude product. The product was recrystallized from ether/hexane to produce 4β-bromo-24,24-difluoro-25-hydroxy-5β-cholestan-3-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04284577 |
| Source dataset | uspto-grants-1981_08 |
| ORD ID | ord-c452aa94590643a2baa50b2333c11f4b |
| Source note | uspto-grants-1981_08 |