Ethanol → N-(3-isopropoxypropyl)-N'-(2-octyl)-p-phenylenediamine

HRID 1658449ノート

反応式

HRID 1658449 の反応式
[CH:1]([O:4][CH2:5][CH2:6][CH2:7][NH:8][C:9]1[CH:14]=[CH:13][C:12]([NH2:15])=[CH:11][CH:10]=1)([CH3:3])[CH3:2].[CH3:16][CH:17](Br)[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23].C(=O)([O-])[O-].[Na+].[Na+].C(O)C>O>[CH:1]([O:4][CH2:5][CH2:6][CH2:7][NH:8][C:9]1[CH:14]=[CH:13][C:12]([NH:15][CH:17]([CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH3:23])[CH3:16])=[CH:11][CH:10]=1)([CH3:3])[CH3:2]

参加物

6

実験手順

A mixture of 50 g. of N-(3-isopropoxypropyl)-p-phenylenediamine, 50 g. of 2-octyl bromide, 200 ml. of 2N sodium carbonate and 1 liter of ethanol is stirred for 18 hours at 60°C. The reaction mixture is treated with 1 liter of water and extracted with 1 liter of ether. The ether layer is separated, washed with 1200 ml. of water, dried over sodium sulfate and evaporated in vacuo. A mixture of the residue in ether is treated with hydrogen chloride gas to yield the title product in dihydrochloride salt form, m.p. 200°-202°C.

後処理

  1. additionA mixture of 50 g
  2. extractionextracted with 1 liter of ether
  3. customThe ether layer is separated
  4. washwashed with 1200 ml
  5. dry with materialof water, dried over sodium sulfate
  6. customevaporated in vacuo
  7. additionA mixture of the residue in ether
  8. additionis treated with hydrogen chloride gas

出典と根拠

ORDレコード
ord-b7c96a907a3a4aa2af5df0a06d2a85f6
出典データセット
uspto-grants-1976_06
特許番号
US03963780

反応ノート

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