Acetic Acid → 1,3-Dichloro-2-(heptafluoropropyl)propan-2-ol

온도

-20 °C

Heptafluoropropyliodide (5 g, 6.9 mmole) was stirred at -78° C. in dry diethylether (20 ml). A solution of phenylmagnesium bromide in ethyl ether (10 ml of a 1.88 M solution) was added over a half-hour period. When this addition was complete, the reaction mixture was stirred at -20° C. for one hour. To this solution was added, at -78° C., 1,3-dichloroacetone (3.25 g, 25.6 mmole) in dry diethylether (20 ml) dropwise, keeping the temperature below -65° C. The mixture was then stirred four hours between -20° and -50° C. Glacial acetic acid (3 ml) in diethylether (5 ml) was added slowly followed by water (15 ml). The mixture was allowed to warm to 5° C. and then the phases were separated. The aqueous phase was washed with ether (2×25 ml). The ethereal extracts were combined, dried (MgSO4) and evaporated to give crude 1,3-dichloro-2-(heptafluoropropyl)propan-2-ol, which was used directly in the next step.

1. additionWhen this addition
2. additionTo this solution was added, at -78° C.
3. customthe temperature below -65° C
4. stirringThe mixture was then stirred four hours between -20° and -50° C
5. temperatureto warm to 5° C.
6. customthe phases were separated
7. washThe aqueous phase was washed with ether (2×25 ml)
8. dry with materialdried (MgSO4)
9. customevaporated

ORD 기록

ord-5d7fcbe5c86240539394c2771bceaa93

출처 데이터셋

uspto-grants-1985_12

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US04560697