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

HRID 1658448

Reaktionsgleichung

Reaktionsgleichung von HRID 1658448
[CH3:1][CH:2]([NH:9][C:10]1[CH:15]=[CH:14][C:13]([NH2:16])=[CH:12][CH:11]=1)[CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH:17]([O:20][CH2:21][CH2:22][CH:23]=O)([CH3:19])[CH3:18].[H][H]>CO.[Pt]=S>[CH:17]([O:20][CH2:21][CH2:22][CH2:23][NH:16][C:13]1[CH:14]=[CH:15][C:10]([NH:9][CH:2]([CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8])[CH3:1])=[CH:11][CH:12]=1)([CH3:19])[CH3:18]

Komponenten

6

Versuchsvorschrift

A mixture of 20 g. of N-(2-octyl)-p-phenylenediamine, 14 g. of 3-isopropoxypropionaldehyde and 0.3g. of 5% platinum sulfide on carbon catalyzt is shaken in a rocker bomb at 150°C under 600 psi hydrogen for 5 hours. After allowing the mixture to cool to room temperature, the contents of the bomb are dissolved in methanol and filtered through celite. The filtrate is evaporated in vacuo and the residue is taken up in ether and treated with an excess of dry hydrogen chloride gas. The resulant solid is collected by filtration and recrystallized from methanol-acetone to yield the product N-(3-isopropoxypropyl)-N'-(2-octyl)-p-phenylenediamine in dihydrochloride salt form (mp 200°-202°C).

Aufarbeitung

  1. additionA mixture of 20 g
  2. filtrationfiltered through celite
  3. customThe filtrate is evaporated in vacuo
  4. additiontreated with an excess of dry hydrogen chloride gas
  5. filtrationThe resulant solid is collected by filtration
  6. customrecrystallized from methanol-acetone

Quellen und Nachweise

ORD-Eintrag
ord-e2a2ba1f29a447c89f78d5be3f4f919e
Quelldatensatz
uspto-grants-1976_06
Patentnummer
US03963780

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