Cyanuric chloride → 2,2,6,6-Tetramethyl-4-octylaminopiperidine

HRID 1709353Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1709353
N1C(Cl)=NC(Cl)=N[C:2]=1Cl.C[C:11]1([CH3:30])[CH2:16][CH:15]([NH:17][CH:18]2[CH2:23][C:22]([CH3:25])([CH3:24])[NH:21][C:20]([CH3:27])([CH3:26])[CH2:19]2)CC(C)(C)N1.Cl[C:32]1N=NN=[C:34](Cl)[CH:33]=1>C1(C)C(C)=CC=CC=1>[CH3:27][C:20]1([CH3:26])[CH2:19][CH:18]([NH:17][CH2:15][CH2:16][CH2:11][CH2:30][CH2:32][CH2:33][CH2:34][CH3:2])[CH2:23][C:22]([CH3:24])([CH3:25])[NH:21]1

Komponenten

5

Edukt 3

HCID 7954Cyanuric chlorideHCID 5667082,2,6,6-Tetramethyl-N-(2,2,6,6-tetramethyl-4-piperidinyl)-4-piperidinamineHCID 18348308Dichlorotriazine

Produkt 1

HCID 143651212,2,6,6-Tetramethyl-4-octylaminopiperidine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7237O-XyleneLösungsmittel

Versuchsvorschrift

The same compound can be obtained by means of a procedure in a single reactor, by reacting 1 mol of cyanuric chloride in xylene first with 1 mol of bis(2,2,6,6-tetramethyl-4-piperidyl)amine and then with 2 mol of 2,2,6,6-tetramethyl-4-octylaminopiperidine without isolation of the dichlorotriazine formed as an intermediate.

Aufarbeitung

  1. customThe same compound can be obtained by means of a procedure in a single reactor

Quellen und Nachweise

ORD-Eintrag
ord-1e5ecf0553c04608ba96a0b36d1ff641
Quelldatensatz
uspto-grants-1990_08
Patentnummer
US04948889

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