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Oxalyl chloride → 5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-2,4-dichlorobenzoyl chloride

HRID 1870095
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HRID 1870095 반응식
[C:1](Cl)(=O)[C:2]([Cl:4])=[O:3].[Cl:7][C:8]1[C:9]([C:18]2[C:19]([Cl:28])=[CH:20][C:21]([Cl:27])=C([CH:26]=2)C(O)=O)=[N:10][N:11]([CH3:17])[C:12]=1[O:13][CH:14]([F:16])[F:15]>C1(C)C=CC=CC=1>[Cl:7][C:8]1[C:9]([C:18]2[C:19]([Cl:28])=[CH:20][C:21]([Cl:27])=[C:1]([CH:26]=2)[C:2]([Cl:4])=[O:3])=[N:10][N:11]([CH3:17])[C:12]=1[O:13][CH:14]([F:16])[F:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 65578Oxalyl chlorideHCID 150305955-(4-Chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-2,4-dichlorobenzoic acid

생성물 1

HCID 153463895-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-2,4-dichlorobenzoyl chloride

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

20.5 g (160 mmol) of oxalyl chloride were added dropwise to a solution of 7.7 g (20 mmol) of 5-(4-chloro-5-difluoromethoxy-1-methyl-1H-pyrazol-3-yl)-2,4-dichlorobenzoic acid in 300 ml of toluene. After 6 hours stirring at reflux temperature, the reaction mixture was concentrated. Yield: quantitative.

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후처리

  1. temperatureat reflux temperature
  2. concentrationthe reaction mixture was concentrated

출처 및 근거

ORD 기록
ord-f54baa8d39764597a58a5aa4797b4c37
출처 데이터셋
uspto-grants-2000_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06096689

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