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2-Chloro-4-[(1-isopropyl-4-piperidinyl)oxy]benzoic acid hydrochloride → 2-Chloro-4-[(1-isopropyl-4-piperidinyl)oxy]benzoyl chloride hydrochloride

HRID 268726
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인쇄 미리보기

반응식

HRID 268726 반응식
[ClH:1].[Cl:2][C:3]1[CH:11]=[C:10]([O:12][CH:13]2[CH2:18][CH2:17][N:16]([CH:19]([CH3:21])[CH3:20])[CH2:15][CH2:14]2)[CH:9]=[CH:8][C:4]=1[C:5](O)=[O:6]>S(Cl)(Cl)=O>[ClH:2].[Cl:2][C:3]1[CH:11]=[C:10]([O:12][CH:13]2[CH2:18][CH2:17][N:16]([CH:19]([CH3:21])[CH3:20])[CH2:15][CH2:14]2)[CH:9]=[CH:8][C:4]=1[C:5]([Cl:1])=[O:6]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 689653592-Chloro-4-[(1-isopropyl-4-piperidinyl)oxy]benzoic acid hydrochloride

생성물 1

HCID 179862952-Chloro-4-[(1-isopropyl-4-piperidinyl)oxy]benzoyl chloride hydrochloride수율 199%

시약·촉매·용매 1

HCID 24386Thionyl Chloride용매

실험 절차

2-Chloro-4-[(1-isopropyl-4-piperidinyl)oxy]benzoic acid hydrochloride (D32) (0.20 g) was dissolved in thionyl chloride (10 ml) and heated under reflux for 1.5 h. The thionyl chloride was removed by evaporation and the residue was evaporated from DCM (3×10 ml) to give the title compound (D33) (0.21 g).

후처리

  1. temperatureheated
  2. temperature
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
under reflux for 1.5 h
  • customThe thionyl chloride was removed by evaporation
  • customthe residue was evaporated from DCM (3×10 ml)
  • 출처 및 근거

    ORD 기록
    ord-b960ebdff33d4014992a20882e199273
    출처 데이터셋
    uspto-grants-2008_11
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07446103B2

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