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Thionyl Chloride → 2-(Octyloxy)propanoyl chloride

HRID 1680989
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HRID 1680989 반응식
[CH2:1]([O:9][CH:10]([CH3:14])[C:11](O)=[O:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].S(Cl)([Cl:17])=O>>[CH2:1]([O:9][CH:10]([CH3:14])[C:11]([Cl:17])=[O:12])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24386Thionyl ChlorideHCID 19807849HCID 19807849, 화합물

생성물 1

HCID 190183272-(Octyloxy)propanoyl chloride

실험 절차

10 ml of thionyl chloride was added to 2.0 g of α-octyloxypropionic acid, and the mixture was refluxed under heat for 2 hours. Then, excess of thionyl chloride was distilled off to obtain α-octyloxypropionic acid chloride. 20 ml of dry pyridine was added thereto, and a solution of 5.0 g of p-hydroxybenzoic acid dissolved in 40 ml of dry pyridine was further added. After the addition, the mixture was refluxed for 2 hours, charged into ice water, and extracted with benzene. The extract was purified with a silica gel column chromatography to obtain 4-α-octyloxypropanoyloxybenzoic acid.

후처리

  1. temperaturethe mixture was refluxed
  2. temperatureunder heat for 2 hours
  3. distillationThen, excess of thionyl chloride was distilled off

출처 및 근거

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
ORD 기록
ord-54b7d832d8094a0cb3d8611eeab3f909
출처 데이터셋
uspto-grants-1992_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05167857

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