반응식
[N:1]1([C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15]([F:18])([F:17])[F:16])=[O:8])[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[ClH:19]>>[ClH:19].[N:1]1([C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=2[C:15]([F:17])([F:16])[F:18])=[O:8])[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1참가 물질
3
반응 조건
- 온도
- 0 °C
실험 절차
Ethereal HCl (30 mL) was added to piperazin-1-yl-(2-trifluoromethyl-phenyl)-methanone (5.5 g, 21.40 mmol) and the resulting mixture was stirred at 0° C. for 30 minutes. The ether was then evaporated to afford 5.7 g (91% yield) of piperazin-1-yl-(2-trifluoromethyl-phenyl)-methanone hydrochloride.
후처리
- customThe ether was then evaporated
출처 및 근거
- ORD 기록
- ord-c33fd48809b94a23b094906311021c33
- 출처 데이터셋
- uspto-grants-2010_11
- 특허 번호
- US07842696B2
연결된 노트
불러오는 중…