Phosphorus oxychloride → 2-(3-Bromophenyl)-4-(chloromethyl)-5-methyl-1,3-oxazole
반응식
[Br:1][C:2]1[CH:3]=[C:4]([C:8]2[O:9][C:10]([CH3:15])=[C:11]([CH3:14])[N+:12]=2[O-])[CH:5]=[CH:6][CH:7]=1.P(Cl)(Cl)([Cl:18])=O>C(Cl)(Cl)Cl>[Br:1][C:2]1[CH:3]=[C:4]([C:8]2[O:9][C:10]([CH3:15])=[C:11]([CH2:14][Cl:18])[N:12]=2)[CH:5]=[CH:6][CH:7]=1참가 물질
실험 절차
A solution of 2-(3-bromophenyl)-4,5-dimethyloxazole-3-oxide (96.6 g, 0.36 mol) in CHCl3 (0.90 L) was treated dropwise with phosphorous oxychloride (61.1 g, 0.40 mol) allowing the reaction to exotherm and then stirred at reflux for 30 min. The reaction was then cooled to room temperature and washed with water (2×1 L). The combined aqueous washes were back extracted with CH2Cl2 (2×400 mL). The organic layers were dried (MgSO4), and the solvent removed in vacuo to give crude product that was recrystallized from hot hexanes (300 mL), decanting the hot supernate away from a dark oily material. The remaining dark oil was agitated in additional hot hexanes (200 mL) and the combined supernates were cooled to 0° C. to crystallize the product which was isolated by filtration to give 74.2 g (72%) of 2-(3-bromophenyl)-4-(chloromethyl)-5-methyloxazole as a lime-green powder. 1H NMR (300 MHz, d6-DMSO) δ8.19 (s, 1H), 7.93 (d, J=8.0 Hz, 1H), 7.58 (d, J=8.0 Hz, H), 7.35 (t, J=8.0 Hz, 1H), 4.45 (s, 2H), 2.41 (s, 3H).
후처리
- customthe reaction
- temperatureat reflux for 30 min
- washwashed with water (2×1 L)
- extractionThe combined aqueous washes were back extracted with CH2Cl2 (2×400 mL)
- dry with materialThe organic layers were dried (MgSO4)
- customthe solvent removed in vacuo
- customto give crude product that
- customwas recrystallized from hot hexanes (300 mL)
- customdecanting the hot supernate away from a dark oily material
- stirringThe remaining dark oil was agitated in additional hot hexanes (200 mL)
- temperaturethe combined supernates were cooled to 0° C.
- customto crystallize the product which
- customwas isolated by filtration
출처 및 근거
- ORD 기록
- ord-6fda9ee49354473db3c790e77c2fe94f
- 출처 데이터셋
- uspto-grants-2003_08
- 특허 번호
- US06610696B2
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