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Thionyl Chloride → 4-(Chlorocarbonyl)phenyl nonanoate

HRID 2372669
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HRID 2372669 반응식
[CH2:1]([C:9]([O:11][C:12]1[CH:20]=[CH:19][C:15]([C:16](O)=[O:17])=[CH:14][CH:13]=1)=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].S(Cl)([Cl:23])=O>C(Cl)(Cl)(Cl)Cl>[CH2:1]([C:9]([O:11][C:12]1[CH:20]=[CH:19][C:15]([C:16]([Cl:23])=[O:17])=[CH:14][CH:13]=1)=[O:10])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24386Thionyl ChlorideHCID 35638214-(Nonanoyloxy)benzoic acid

생성물 1

HCID 135310434-(Chlorocarbonyl)phenyl nonanoate

시약·촉매·용매 1

HCID 5943Carbon Tetrachloride용매

실험 절차

2.5 g of 4-octylcarbonyloxybenzoic acid was dispersed in 50 ml carbon tetrachloride, after dropping 10 ml of thionyl chloride to this solution, refluxed for three hours. After reducing the solvent, 4-octylcarbonyloxybenzoic chloride (CK) was obtained.

후처리

  1. temperaturerefluxed for three hours

출처 및 근거

ORD 기록
ord-9798d60ffc9a4a22a11c8ca7d6213637
출처 데이터셋
uspto-grants-1992_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05100579

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