반응식
[C:1]1([CH:7]([C:9]2[CH:18]=[C:17]3[C:12]([CH:13]=[CH:14][CH:15]=[N:16]3)=[CH:11][CH:10]=2)O)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.S(Cl)([Cl:21])=O>ClCCl>[Cl:21][CH:7]([C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1)[C:9]1[CH:18]=[C:17]2[C:12]([CH:13]=[CH:14][CH:15]=[N:16]2)=[CH:11][CH:10]=1참가 물질
4
실험 절차
A mixture of 3.2 parts of intermediate 2, namely α-phenyl-7-quinolinemethanol, 8 parts of thionyl chloride and 65 parts of dichloromethane was stirred for 4 hours at room temperature. The reaction mixture was evaporated and the residue was poured into water. The product was extracted with dichloromethane (3×39 parts) and the combined extracts were dried, filtered and evaporated, yielding 3.4 parts (98.5%) of 7-(chlorophenylmethyl)quinoline (interm. 23).
후처리
- customThe reaction mixture was evaporated
- additionthe residue was poured into water
- extractionThe product was extracted with dichloromethane (3×39 parts)
- customthe combined extracts were dried
- filtrationfiltered
- customevaporated
출처 및 근거
- ORD 기록
- ord-8779671dda924d9d8ed4e10f305c4108
- 출처 데이터셋
- uspto-grants-1993_12
- 특허 번호
- US05268380
연결된 노트
불러오는 중…