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Hydrochloric Acid → 1-Methyl-2-{2-[2-(2-phenylethyl)phenoxy]ethyl}piperidine hydrochloride

HRID 743292
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HRID 743292 반응식
[ClH:1].[CH3:2][N:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH:4]1[CH2:9][CH2:10][O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.C(OCC)(=O)C>O1CCOCC1>[ClH:1].[CH3:2][N:3]1[CH2:8][CH2:7][CH2:6][CH2:5][CH:4]1[CH2:9][CH2:10][O:11][C:12]1[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=1[CH2:18][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 8857Ethyl AcetateHCID 108323431-Methyl-2-{2-[2-(2-phenylethyl)phenoxy]ethyl}piperidine

생성물 1

HCID 574976321-Methyl-2-{2-[2-(2-phenylethyl)phenoxy]ethyl}piperidine hydrochloride수율 47%

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

0.6 ml of a 4N solution of hydrogen chloride in dioxane was added to a solution of 670 mg of 1-methyl-2-{2-[2-(2-phenylethyl)phenoxy]ethyl}piperidine [prepared as described in step (a) above] in a suitable amount of ethyl acetate, and the resulting mixture was concentrated by distillation under reduced pressure. The resulting solid residue was recrystallized from ethyl acetate, to give 350 mg (yield 47%) of the title compound as colorless crystals, melting at 128°-130° C.

후처리

  1. concentrationthe resulting mixture was concentrated by distillation under reduced pressure
  2. customThe resulting solid residue was recrystallized from ethyl acetate

출처 및 근거

ORD 기록
ord-dc52cc8620d14d2aa1db20132d4b0a5c
출처 데이터셋
uspto-grants-1996_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05556864

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