반응식
Br[C:2]([F:6])=[C:3]([F:5])[F:4].C(=O)=O.[CH3:10][O:11][CH2:12][CH2:13][CH:14]([C:16]1[CH:21]=[CH:20][C:19]([Cl:22])=[CH:18][CH:17]=1)Br>CN(C)C=O.CC1CC[C@@H](C(C)=C)CC=1.[Zn]>[Cl:22][C:19]1[CH:18]=[CH:17][C:16]([CH:14]([CH2:13][CH2:12][O:11][CH3:10])[C:2]([F:6])=[C:3]([F:5])[F:4])=[CH:21][CH:20]=1참가 물질
반응 조건
- 온도
- 60 °C
실험 절차
Bromotrifluoroethylene (41.5 g, 257 mmol) was distilled (dry ice condenser) into a flask containing zinc (13.6 g, 208 mmol) and N,N-dimethylformamide (153 ml), and the resulting mixture was heated at approximately 60° C. for two hours. The reaction mixture was purged with nitrogen for one hour, cooled to −8° C., treated with cuprous bromide (29.83 g, 208 mmol), and stirred for 30 minutes without external cooling. 3-(4-chlorophenyl)-3-bromopropyl methyl ether (17.06 g, 64.7 mmol) in N,N-dimethylformamide (10 ml) was added followed by limonene (5 drops), and the resulting mixture was heated at 50° C. for 8 hours. The cooled reaction mixture was quenched with aqueous ammonium chloride and thoroughly extracted with hexane. The combined organic extracts were dried over anhydrous sodium sulfate and concentrated in vacuo to a brown oil (10.76 g). Chromatography on silica gel eluting with methylene chloride:hexane (1:9) afforded the title compound as a yellow oil (2.25 g), which was characterized by IR, 1HNMR and mass spectral analysis.
후처리
- customThe reaction mixture was purged with nitrogen for one hour
- temperaturecooled to −8° C.
- temperaturethe resulting mixture was heated at 50° C. for 8 hours
- customThe cooled reaction mixture
- customwas quenched with aqueous ammonium chloride
- extractionthoroughly extracted with hexane
- dry with materialThe combined organic extracts were dried over anhydrous sodium sulfate
- concentrationconcentrated in vacuo to a brown oil (10.76 g)
출처 및 근거
- ORD 기록
- ord-e561f314e7744366a11168dbac168c4f
- 출처 데이터셋
- uspto-grants-2003_01
- 특허 번호
- US06506800B2
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