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3,4-Dichlorobenzaldehyde → 5-(4-(3,4-Dichlorobenzylideneamino)phenyl)thiazolidine-2,4-dione

HRID 1742827
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인쇄 미리보기

반응식

HRID 1742827 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]2[S:12][C:11](=[O:13])[NH:10][C:9]2=[O:14])=[CH:4][CH:3]=1.[Cl:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][C:23]=1[Cl:24])[CH:19]=O>C(O)C>[Cl:15][C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][C:23]=1[Cl:24])[CH:19]=[N:1][C:2]1[CH:3]=[CH:4][C:5]([CH:8]2[S:12][C:11](=[O:13])[NH:10][C:9]2=[O:14])=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 227103,4-DichlorobenzaldehydeHCID 128509725-(4-Aminophenyl)thiazolidine-2,4-dione

생성물 1

HCID 190060585-(4-(3,4-Dichlorobenzylideneamino)phenyl)thiazolidine-2,4-dione수율 90.1%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Into 20 ml of ethanol were suspended 0.50 g of 5-(4-aminophenyl)-thiazolidine-2,4-dione, and, after added 0.42 g of 3,4-dichlorobenzaldehyde thereto, the suspension was refluxed for 3 hours. After cooling by standing, the crystals deposited were collected by filtration. The crude crystals were recrystallized from ethanol to obtain 0.79 g of title compound.

후처리

  1. temperaturethe suspension was refluxed for 3 hours
  2. temperatureAfter cooling
  3. filtrationthe crystals deposited were collected by filtration
  4. customThe crude crystals were recrystallized from ethanol

출처 및 근거

ORD 기록
ord-e9a02d51738344c3a0c7633f27cc843d
출처 데이터셋
uspto-grants-1994_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05342850

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