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Water → 4-[(2,4-Dichlorobenzoyl)amino]-2-chlorobenzoic acid

HRID 55210
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인쇄 미리보기

반응식

HRID 55210 반응식
[Cl:1][C:2]1[CH:10]=[C:9]([NH2:11])[CH:8]=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].C(N(CC)C(C)C)(C)C.[Cl:21][C:22]1[CH:29]=[C:28]([Cl:30])[CH:27]=[CH:26][C:23]=1[CH2:24]Cl.[OH2:31]>C(Cl)Cl>[Cl:21][C:22]1[CH:29]=[C:28]([Cl:30])[CH:27]=[CH:26][C:23]=1[C:24]([NH:11][C:9]1[CH:8]=[CH:7][C:3]([C:4]([OH:6])=[O:5])=[C:2]([Cl:1])[CH:10]=1)=[O:31]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 72122,4-Dichlorobenzyl chlorideHCID 171544-Amino-2-chlorobenzoic acidHCID 81531Diisopropylethylamine

생성물 1

HCID 218369754-[(2,4-Dichlorobenzoyl)amino]-2-chlorobenzoic acid

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

To a stirred mixture of 5.19 g of 2-chloro-4-aminobenzoic acid in 150 ml of methylene chloride is added 7.86 g of N,N-diisopropylethylamine and 12.67 g of 2,4-dichlorobenzylchloride and stirring continued for 18 hours. Water is added to the filtrate and the organic layer dried with Na2SO4 and concentrated in vacuo to give 13.68 g of the desired product, m.p. 171°-175° C.

후처리

  1. dry with materialthe organic layer dried with Na2SO4
  2. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-2c6344183756424e98f2f44acba664c9
출처 데이터셋
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05624923

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