반응식
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([CH2:10][Br:11])=[N:7][C:6]=2[CH:12]=1.[C:13]1([P:19]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>CC#N.CCOCC>[Br-:11].[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([CH2:10][P+:19]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[C:13]3[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=3)=[N:7][C:6]=2[CH:12]=1참가 물질
5
실험 절차
A solution of the bromide (500 mg) (Step 3) and triphenylphosphine (740 mg) in CH3CN (5 mL) was stirred at room temperature overnight. The reaction mixture was diluted with Et2O (20 mL), stirred for 30 min, and filtered to give the title compound as a white solid.
후처리
- filtrationfiltered
출처 및 근거
- ORD 기록
- ord-07367f49a302496b9fb474ee9f3acff1
- 출처 데이터셋
- uspto-grants-1990_09
- 특허 번호
- US04957932
연결된 노트
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