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

HRID 482154Notes

Reaction equation

HRID 482154 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-1ec086fd43ac4f5a8e3f3a4383e46171
Source dataset
uspto-grants-1998_08
Patent number
US05792863

Reaction notes

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