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Aniline → N-(3,4-Dichloro-phenyl)-2-phenylamino-acetamide

HRID 732962
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반응식

HRID 732962 반응식
Br[CH2:2][C:3]([NH:5][C:6]1[CH:11]=[CH:10][C:9]([Cl:12])=[C:8]([Cl:13])[CH:7]=1)=[O:4].[NH2:14][C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=1.C(N(C(C)C)C(C)C)C>C1COCC1>[Cl:13][C:8]1[CH:7]=[C:6]([NH:5][C:3](=[O:4])[CH2:2][NH:14][C:15]2[CH:20]=[CH:19][CH:18]=[CH:17][CH:16]=2)[CH:11]=[CH:10][C:9]=1[Cl:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6115AnilineHCID 81531DiisopropylethylamineHCID 34147142-bromo-N-(3,4-dichlorophenyl)acetamide

생성물 1

HCID 4013057N-(3,4-Dichloro-phenyl)-2-phenylamino-acetamide수율 1,000.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To 2-bromo-N-(3,4-dichloro-phenyl)-acetamide (2 g) in THF (80 mL) was added aniline (41 mg) and N-ethyldiisopropylamine and the reaction mixture was stirred over night at reflux. The precipitated salt was then filtered off and the filtrate was then concentrated in vacuo. The residue was then purified by column chromatography to give the title compound as a light brown solid (1.3 g, mp=110-112° C.).

후처리

  1. temperatureat reflux
  2. filtrationThe precipitated salt was then filtered off
  3. concentrationthe filtrate was then concentrated in vacuo
  4. customThe residue was then purified by column chromatography

출처 및 근거

ORD 기록
ord-4fb9c061612d47e7be6cf8c1001922d4
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07589089B2

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