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Ethylenediamine → N-(4-chlorobenzyl)ethane-1,2-diamine

HRID 236010
ノート
印刷プレビュー

反応式

HRID 236010 の反応式
[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6]Cl)=[CH:4][CH:3]=1.[CH2:10]([NH2:13])[CH2:11][NH2:12].[OH-].[Na+]>O>[Cl:1][C:2]1[CH:9]=[CH:8][C:5]([CH2:6][NH:12][CH2:11][CH2:10][NH2:13])=[CH:4][CH:3]=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 3301EthylenediamineHCID 77231-Chloro-4-(chloromethyl)benzeneHCID 14798Sodium Hydroxide

生成物 1

HCID 13785698N-(4-chlorobenzyl)ethane-1,2-diamine

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

p-Chlorobenzyl chloride, 32 g. (0.2 mole), was added dropwise to 60 g. (1.0 mole) of ethylenediamine heated at 80°. The solution was stirred at 80° overnight and then the excess amine was distilled in vacuo. The residue was triturated with i-PrOH to yield 32 g. of crude product. This material was dissolved in water, basified with dilute NaOH and the solution extracted with CH2Cl2. The combined extracts were dried (K2CO3) and concentrated in vacuo to an oil. The latter was distilled and the material boiling at 93°-95°/0.06 mm Hg was collected to yield 14.5 g. of the desired product, the identity of which was confirmed by examination of the NMR spectrum.

このページの内容参加物実験手順後処理出典と根拠反応ノート

後処理

  1. addition(0.2 mole), was added dropwise to 60 g
  2. distillationthe excess amine was distilled in vacuo
  3. customThe residue was triturated with i-PrOH
  4. customto yield 32 g
  5. extractionthe solution extracted with CH2Cl2
  6. dry with materialThe combined extracts were dried (K2CO3)
  7. concentrationconcentrated in vacuo to an oil
  8. distillationThe latter was distilled
  9. customthe material boiling at 93°-95°/0.06 mm Hg was collected
  10. customto yield 14.5 g

出典と根拠

ORDレコード
ord-8ddd2b48c46e45acaa8e829b3f213434
出典データセット
uspto-grants-1987_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04642345

反応ノート

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