HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-Bromo-2,6-dichloro-6-fluorocyclohexanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Boron tribromide | HCID 25134 | — |
| Reactant | 1,3-Dichloro-3-fluoro-7-oxabicyclo[4.1.0]heptane | HCID 18970966 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Bromo-2,6-dichloro-6-fluorocyclohexanol | HCID 18970968 | — |
Reaction Steps
2.91 cm3 (2.91 mmol) of BBr3 in molar solution in dichloromethane were introduced at 4° C. under argon atmosphere into 0.98 (5.3 mmol) of epoxide 2e in solution in 6.5 cm3 dichloromethane. The reaction mixture was then allowed to return to room temperature and stirring was continued (1 h 30 min). 5 cm3 of distilled water were then added and the mixture was extracted with dichloromethane (4×10 cm3). The extract was dried over MgSO4, filtered and evaporated down. The crude product was purified by flash chromatography on silica (eluent ether/petroleum ether=5/95): 1.03 g of alcohol 1i were obtained (macrobore GC purity>97%); the yield of product 1i was 73%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05424460 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-a254a47f4a7b42b890ab20256a72c77c |
| Source note | uspto-grants-1995_06 |