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Diethyl Malonate → N~1~,N~3~-bis(2,4-dichlorophenyl)malonamide

HRID 424701
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HRID 424701 반응식
[C:1]([O:9]CC)(=O)[CH2:2][C:3]([O:5]CC)=O.[Cl:12][C:13]1[CH:19]=[C:18]([Cl:20])[CH:17]=[CH:16][C:14]=1[NH2:15]>>[Cl:12][C:13]1[CH:19]=[C:18]([Cl:20])[CH:17]=[CH:16][C:14]=1[NH:15][C:3](=[O:5])[CH2:2][C:1]([NH:15][C:14]1[CH:16]=[CH:17][C:18]([Cl:20])=[CH:19][C:13]=1[Cl:12])=[O:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 7761Diethyl MalonateHCID 111232,4-Dichloroaniline

생성물 1

HCID 3332858N~1~,N~3~-bis(2,4-dichlorophenyl)malonamide

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온도
200 °C

실험 절차

A mixture of diethyl malonate (24 g, 0.15 mol) and 2,4-dichloro aniline (60.8 g, 2.5 eq) was heated at 200° C. upon passing nitrogen gas stream to distil out ethanol. Six hours later, the reactants were cooled to room temperature with adding diethylether. The solids produced were filtered and washed with diethylether (yield: 48 g, 82%): 1H NMR (CDCl3) δ10.04 (s, 2H) 8.04 (d, J=9 Hz, 2H) 7.42 (m, 2H) 7.26, (dd, J=2.4, 9 Hz, 2H) 3.74 (s, 2H)

후처리

  1. customto distil out ethanol
  2. temperatureSix hours later, the reactants were cooled to room temperature with adding diethylether
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
custom
The solids produced
  • filtrationwere filtered
  • washwashed with diethylether (yield: 48 g, 82%)
  • 출처 및 근거

    ORD 기록
    ord-905c8b8d65d24a0e92c193ad2019a0db
    출처 데이터셋
    uspto-grants-2012_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08106071B2

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