Ethanol → n,n-Di(2-ethylhexyl)-p-phenylenediamine

HRID 443028Notes

Reaction equation

HRID 443028 reaction equation
[OH-].[Na+].C([NH:6][C:7]1[CH:12]=[CH:11][C:10]([N:13]([CH2:22][CH:23]([CH2:28][CH3:29])[CH2:24][CH2:25][CH2:26][CH3:27])[CH2:14][CH:15]([CH2:20][CH3:21])[CH2:16][CH2:17][CH2:18][CH3:19])=[CH:9][CH:8]=1)(=O)C.C(O)C>O>[CH2:20]([CH:15]([CH2:16][CH2:17][CH2:18][CH3:19])[CH2:14][N:13]([CH2:22][CH:23]([CH2:28][CH3:29])[CH2:24][CH2:25][CH2:26][CH3:27])[C:10]1[CH:9]=[CH:8][C:7]([NH2:6])=[CH:12][CH:11]=1)[CH3:21]

Participants

5

Procedure

A mixed solution comprising 8 ml of 30% sodium hydroxide solution, 1.012 g of N-acetyl-N',N'-di(2-ethylhexyl)-p-phenylenediamine and 10 ml of ethanol was allowed to react at 75° C. for a period of 5 hr. After the completion of the reaction, the reacted solution was introduced into water and the product was extracted by ethyl acetate. After ethyl acetate was distilled away, the residue was purified by silica gel column chromatography to obtain 501 mg of oil of N,N-di(2-ethylhexyl)-p-phenylenediamine (yield 53.4%).

Workup

  1. customto react at 75° C. for a period of 5 hr
  2. customAfter the completion of the reaction
  3. extractionthe product was extracted by ethyl acetate
  4. distillationAfter ethyl acetate was distilled away
  5. customthe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-e23238fde8a04b409f275632273ac9ad
Source dataset
uspto-grants-1999_04
Patent number
US05892042

Reaction notes

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