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Thionyl Chloride → 4-(3-Diethylaminopropoxy)benzoyl chloride

HRID 346877
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HRID 346877 반응식
[CH2:1]([N:3]([CH2:17][CH3:18])[CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:16]=[CH:15][C:11]([C:12](O)=[O:13])=[CH:10][CH:9]=1)[CH3:2].S(Cl)([Cl:21])=O>C(Cl)Cl>[CH2:1]([N:3]([CH2:4][CH2:5][CH2:6][O:7][C:8]1[CH:16]=[CH:15][C:11]([C:12]([Cl:21])=[O:13])=[CH:10][CH:9]=1)[CH2:17][CH3:18])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 176070464-(3-(Diethylamino)propoxy)benzoic acid

생성물 1

HCID 214352614-(3-Diethylaminopropoxy)benzoyl chloride

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

A solution of the compound from Example 2(ii)(6 g, 24 mmol) in DCM was stirred at 0° C. Thionyl chloride was added drop-wise and the reaction was heated at reflux for 24 hrs. The reaction was allowed to cool and the solvents removed under vacuum to afford the expected compound as a pungent crude solid. 5.9 g, 100%. The solid was used without further purification.

후처리

  1. temperaturethe reaction was heated
  2. temperatureat reflux for 24 hrs
  3. temperatureto cool
  4. customthe solvents removed under vacuum

출처 및 근거

ORD 기록
ord-8e2e87e7931545c7ac0028b3f0c20262
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07173061B2

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