Thionyl Chloride → HCID 12010380, 화합물
반응식
O[CH2:2][C:3]1[N:4]=[C:5]([C:8]2[CH:13]=[C:12]([O:14][CH3:15])[C:11]([O:16][CH3:17])=[C:10]([O:18][CH3:19])[CH:9]=2)[S:6][CH:7]=1.S(Cl)([Cl:22])=O>ClCCl>[Cl:22][CH2:2][C:3]1[N:4]=[C:5]([C:8]2[CH:13]=[C:12]([O:14][CH3:15])[C:11]([O:16][CH3:17])=[C:10]([O:18][CH3:19])[CH:9]=2)[S:6][CH:7]=1참가 물질
4
실험 절차
4-Hydroxymethyl-2-(3,4,5-trimethoxyphenyl)thiazole (2.0 g) was dissolved in dichloromethane (60 mL), and to the solution thionyl chloride (1.1 g) was added at 0° C. After 30 minutes, the mixture was warmed to room temperature and stirred for 4 hours. The reaction mixture was washed with water and saturated brine and dried over anhydrous sodium sulfate. After concentrating the reaction mixture under reduced pressure, the resultant crude crystals were recrystallized from chloroform-hexane to obtain the title compound.
후처리
- washThe reaction mixture was washed with water and saturated brine
- dry with materialdried over anhydrous sodium sulfate
- concentrationAfter concentrating the reaction mixture under reduced pressure
- customthe resultant crude crystals were recrystallized from chloroform-hexane
출처 및 근거
- ORD 기록
- ord-8adfac5c3aec49198ad8a4b90cf5a1db
- 출처 데이터셋
- uspto-grants-2002_10
- 특허 번호
- US06472386B1
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