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N,N'-Dimethylethylenediamine → N~1~-(Diphenylmethyl)-N~1~,N~2~-dimethylethane-1,2-diamine

HRID 2251951
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인쇄 미리보기

반응식

HRID 2251951 반응식
[CH3:1][NH:2][CH2:3][CH2:4][NH:5][CH3:6].C(=O)([O-])[O-].[K+].[K+].[CH:13](Br)([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1>CN(C=O)C>[CH:13]([N:2]([CH3:1])[CH2:3][CH2:4][NH:5][CH3:6])([C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 8070N,N'-DimethylethylenediamineHCID 11430Potassium CarbonateHCID 236603Bromodiphenylmethane

생성물 1

HCID 13984386N~1~-(Diphenylmethyl)-N~1~,N~2~-dimethylethane-1,2-diamine

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

15.1 g (171 mmol) N,N′-dimethylethylenediamine, 35 g (255 mmol) potassium carbonate are placed in 250 ml DMF and 30.9 g (125 mmol) benzhydryl bromide are added dropwise at RT. The mixture is concentrated under vacuum. The residue is taken up in chloroform and washed with water. The organic phase is dried over sodium sulfate and the solvent is removed under vacuum. The purification occurs by chromatography on silica gel with chloroform: Yield 14.5 g (45%).

후처리

  1. concentrationThe mixture is concentrated under vacuum
  2. washwashed with water
  3. dry with materialThe organic phase is dried over sodium sulfate
  4. customthe solvent is removed under vacuum
  5. customThe purification

출처 및 근거

ORD 기록
ord-85ba89e49b8c49ecb4ccd358a01b2230
출처 데이터셋
uspto-grants-2008_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07320993B1

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