Ethyl formate → 4-(N-formyl-N-octylamino)-2,2,6,6-tetramethylpiperidine

HRID 1110688

Reaktionsgleichung

Reaktionsgleichung von HRID 1110688
[CH2:1]([NH:9][CH:10]1[CH2:15][C:14]([CH3:17])([CH3:16])[NH:13][C:12]([CH3:19])([CH3:18])[CH2:11]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8].[CH:20](OCC)=[O:21]>CCCCO.CCCCO.CCCCO.CCCCO.[Ti]>[CH2:1]([N:9]([CH:10]1[CH2:11][C:12]([CH3:18])([CH3:19])[NH:13][C:14]([CH3:17])([CH3:16])[CH2:15]1)[CH:20]=[O:21])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH3:8]

Komponenten

4

Edukt 2

HCID 8025Ethyl formateHCID 143651212,2,6,6-Tetramethyl-4-octylaminopiperidine

Produkt 1

HCID 144190584-(N-formyl-N-octylamino)-2,2,6,6-tetramethylpiperidine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 521701TetrabutoxytitaniumKatalysator

Versuchsvorschrift

93 g of 4-(N-octylamino)-2,2,6,6-tetramethylpiperidine and 33 g of tetrabutyl orthotitanate in 175 ml of ethyl formate were refluxed for 10.5 hours. Working up as in Example 2 gave 4-(N-octyl-N-formylamino)-2,2,6,6-tetramethylpiperidine as a colorless oil of boiling point 145°-147° C./0.5 mmHg

Quellen und Nachweise

ORD-Eintrag
ord-9b92b48365af4c99936c428d83d5fb93
Quelldatensatz
uspto-grants-1990_12
Patentnummer
US04976889

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