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

HRID 971848
ノート
印刷プレビュー

反応式

HRID 971848 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

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

生成物 1

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

試薬・触媒・溶媒 1

HCID 1140Toluene溶媒

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-a514ab7a09994b5487c82e7cac01daef
出典データセット
uspto-grants-1979_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04161528

反応ノート

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