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p-Toluidine → N~1~-(3-Chlorophenyl)-N~2~-(4-methylphenyl)ethane-1,2-diamine

HRID 971848
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HRID 971848 반응식
Br.Br[CH2:3][CH2:4][NH:5][C:6]1[CH:11]=[CH:10][CH:9]=[C:8]([Cl:12])[CH:7]=1.[CH3:13][C:14]1[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=1.C(=O)([O-])[O-].[Na+].[Na+]>C1(C)C=CC=CC=1>[Cl:12][C:8]1[CH:7]=[C:6]([NH:5][CH2:4][CH2:3][NH:18][C:17]2[CH:19]=[CH:20][C:14]([CH3:13])=[CH:15][CH:16]=2)[CH:11]=[CH:10][CH:9]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 7813p-ToluidineHCID 10340Sodium CarbonateHCID 12606987N-(2-Bromoethyl)-3-chloroaniline--hydrogen bromide (1/1)

생성물 1

HCID 21312028N~1~-(3-Chlorophenyl)-N~2~-(4-methylphenyl)ethane-1,2-diamine수율 76.6%

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

A mixture consisting of 15.8 gm of N-(2-bromo-ethyl)-3-chloro-aniline hydrobromide, 10.7 gm of 4-methyl-aniline, 50 ml of toluene and 15 gm of anhydrous sodium carbonate was refluxed for eight hours, while stirring. Thereafter, the reaction mixture was filtered, the filter cake was washed with ethyl acetate, and the filtrate was evaporated in vacuo, leaving 10 gm of an oil which was used as the starting material in Example 11 without further purification. It was identified to be N-(3-chloro-phenyl)-N'-(4-methyl-phenyl)-ethylenediamine.

후처리

  1. temperaturewas refluxed for eight hours
  2. filtrationThereafter, the reaction mixture was filtered
  3. washthe filter cake was washed with ethyl acetate
  4. customthe filtrate was evaporated in vacuo

출처 및 근거

ORD 기록
ord-a514ab7a09994b5487c82e7cac01daef
출처 데이터셋
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04161528

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