Hydrochloric Acid → 4-{2-[2-(3-Methoxyphenyl)ethyl]phenoxy}-1-methylpiperidine hydrochloride
반응식
[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6]([CH2:10][CH2:11][C:12]2[CH:25]=[CH:24][CH:23]=[CH:22][C:13]=2[O:14][CH:15]2[CH2:20][CH2:19][N:18]([CH3:21])[CH2:17][CH2:16]2)[CH:7]=[CH:8][CH:9]=1>O1CCOCC1.C(OCC)(=O)C>[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[C:6]([CH2:10][CH2:11][C:12]2[CH:25]=[CH:24][CH:23]=[CH:22][C:13]=2[O:14][CH:15]2[CH2:20][CH2:19][N:18]([CH3:21])[CH2:17][CH2:16]2)[CH:7]=[CH:8][CH:9]=1참가 물질
5
실험 절차
0.2 ml of a 4N solution of hydrogen chloride in dioxane was added dropwise to a solution of 220 mg of 4-{2-[2-(3-methoxyphenyl)ethyl]phenoxy}-1-methylpiperidine [prepared as described in step (a) above] in 20 ml of ethyl acetate, and the mixture was allowed to stand at room temperature. The crystals which precipitated were collected by filtration and dried in vacuo, to give 170 mg (yield 69%) of the title compound as colorless crystals, melting at 147°-148° C.
후처리
- customto stand at room temperature
- customThe crystals which precipitated
- filtrationwere collected by filtration
- customdried in vacuo
출처 및 근거
- ORD 기록
- ord-51893b3c8af04a8986eb1e6f2dbf65ab
- 출처 데이터셋
- uspto-grants-1996_09
- 특허 번호
- US05556864
반응 노트
불러오는 중…