반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH3:8])[CH:3]=1.N1C=CC=CC=1.[C:15](Cl)(=[O:24])[CH:16]=[CH:17][C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1>ClCCl>[C:4]1([CH3:8])[CH:5]=[CH:6][CH:7]=[C:2]([NH:1][C:15](=[O:24])[CH:16]=[CH:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=2)[CH:3]=1참가 물질
5
반응 조건
- 온도
- 0 °C
실험 절차
m-Toluidine (5 g, 46.64 mmol) and pyridine (3.77 mL, 46.64 mmol) were dissolved in dry dichloromethane (25 mL). To the reaction mixture, cinnamoyl chloride (7.72 g, 46.64 mmol) was added and stirred for 3 h at 0° C. The reaction mixture was extracted with dichloromethane washing with water and 2N HCl. The solvent was removed and the crude product was used in the next step without further purification.
후처리
- extractionThe reaction mixture was extracted with dichloromethane washing with water and 2N HCl
- customThe solvent was removed
- customthe crude product was used in the next step without further purification
출처 및 근거
- ORD 기록
- ord-14ca28f2f70a417195f49f94d34eea8b
- 출처 데이터셋
- uspto-grants-2013_10
- 특허 번호
- US08569282B2
연결된 노트
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