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2,6-Dichlorobenzoyl chloride → HCID 20546750, 화합물

HRID 2059237
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반응식

HRID 2059237 반응식
[F:1][C:2]([F:14])([F:13])[C:3]1[C:11]2[O:10][N:9]=[C:8]([NH2:12])[C:7]=2[CH:6]=[CH:5][CH:4]=1.[Cl:15][C:16]1[CH:24]=[CH:23][CH:22]=[C:21]([Cl:25])[C:17]=1[C:18](Cl)=[O:19]>C1(C)C=CC=CC=1>[Cl:15][C:16]1[CH:24]=[CH:23][CH:22]=[C:21]([Cl:25])[C:17]=1[C:18]([NH:12][C:8]1[C:7]2[CH:6]=[CH:5][CH:4]=[C:3]([C:2]([F:1])([F:13])[F:14])[C:11]=2[O:10][N:9]=1)=[O:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 783922,6-Dichlorobenzoyl chlorideHCID 107744567-Trifluoromethyl-benzo[d]isoxazol-3-ylamine

생성물 1

HCID 20546750HCID 20546750, 화합물

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

7-(Trifluoromethyl)-3-aminobenzisoxazole (2 gram), 2,6-dichlorobenzoylchloride (2 gram), and 50 ml. of toluene are heated at reflux for 16 hours. After evaporation of the solvent at reduced pressure, the resultant oily semi-solid is triturated with ether. The solid so formed is then washed with ether and water and constitutes the desired product.

후처리

  • temperatureat reflux for 16 hours
  • customAfter evaporation of the solvent at reduced pressure
  • customthe resultant oily semi-solid is triturated with ether
  • customThe solid so formed
  • washis then washed with ether and water
  • 출처 및 근거

    ORD 기록
    ord-040ca746202f4b7a9c02a29f90e9d7e2
    출처 데이터셋
    uspto-grants-1982_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04322429

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