Acetic Acid → 3-(2-(4-(1-Methylethyl)-2-thiazolyl)ethenyl)benzaldehyde
반응식
[CH3:1][CH:2]([C:4]1[N:5]=[C:6]([CH3:9])[S:7][CH:8]=1)[CH3:3].C(O[C:14](=[O:16])[CH3:15])(=O)C.C(O)(=O)C.[C:21]1([CH3:27])[CH:26]=C[CH:24]=[CH:23][CH:22]=1>>[CH3:1][CH:2]([C:4]1[N:5]=[C:6]([CH:9]=[CH:27][C:21]2[CH:26]=[C:15]([CH:24]=[CH:23][CH:22]=2)[CH:14]=[O:16])[S:7][CH:8]=1)[CH3:3]참가 물질
5
실험 절차
4-(1-Methylethyl)-2-methylthiazole (546 mg, EP 0219436 p. 19) and isophthaladehyde (570 mg, 1.1 equiv.) are heated at reflux in acetic anhydride (1.1 mL, 3 equiv.) 16 hours. The reaction mixture is cooled and the acetic acid and anhydride are co-evaporated with toluene. The title compound is purified by flash chromatography on silica using EtOAc:hexane 10:90.
후처리
- temperatureThe reaction mixture is cooled
- customThe title compound is purified by flash chromatography on silica
출처 및 근거
- ORD 기록
- ord-c88d99a0ca7245358ebb6512e838011e
- 출처 데이터셋
- uspto-grants-1990_10
- 특허 번호
- US04962117
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