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2-Chloroaniline → HCID 13002203, 화합물

HRID 461671
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HRID 461671 반응식
[CH3:1][C:2]1([CH3:10])[CH2:9][C:7](=[O:8])[CH2:6][C:4](=O)[CH2:3]1.[Cl:11][C:12]1[CH:18]=[CH:17][CH:16]=[CH:15][C:13]=1[NH2:14]>>[Cl:11][C:12]1[CH:18]=[CH:17][CH:16]=[CH:15][C:13]=1[NH:14][C:4]1[CH2:3][C:2]([CH3:1])([CH3:10])[CH2:9][C:7](=[O:8])[CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 72402-ChloroanilineHCID 31358Dimedone

생성물 1

HCID 13002203HCID 13002203, 화합물

실험 절차

A mixture of 40 parts of dimedone and 36.4 parts of 2-chloroaniline is heated at 170°-175° C for 45 minutes, followed by cooling. The resulting reaction product is recrystallized to obtain yellow cubes. The crystals are collected by filtration, washed well with isopropyl ether and recrystallized from acetone. The procedure yields colorless prisms of 3-(2-chloroanilino)-5,5-dimethyl-2-cyclohexen-1-one. Melting point: 150°-152° C. By procedures similar to those described in Example 1 (a) and (b), the following compounds are produced.

후처리

  1. temperatureis heated at 170°-175° C for 45 minutes
  2. temperatureby cooling
  3. customThe resulting reaction product
  4. customis recrystallized
  5. customto obtain yellow cubes
  6. filtrationThe crystals are collected by filtration
  7. wash
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
washed well with isopropyl ether
  • customrecrystallized from acetone
  • 출처 및 근거

    ORD 기록
    ord-ba7943258d204ca7b435c9adf0798429
    출처 데이터셋
    uspto-grants-1977_12
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04064133

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