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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 375773Erstellt: 26. Oktober 2026

n-Butyl-2,2,6,6-tetramethyl-4-piperidinamine → Ethyl N-[2,4-bis(N-butyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino)-1,3,5-triazin-6-yl]glycinate

https://huagongshe.com/reaction/375773

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktn-Butyl-2,2,6,6-tetramethyl-4-piperidinamineHCID 118285—
EduktSodium BicarbonateHCID 516892—
Edukt4,6-dichloro-2-ethoxycarbonylmethylamino-S-triazineHCID 14746261—
LösungsmittelO-XyleneHCID 7237—
ProduktEthyl N-[2,4-bis(N-butyl-N-(2,2,6,6-tetramethyl-4-piperidyl)amino)-1,3,5-triazin-6-yl]glycinateHCID 1474620696,3%

Reaktionsschritte

2.36 g of ethyl N-(2,4-dichloro-1,3,5-triazin-6-yl)glycinate [obtained as described in Preparation 4(A)], 4.19 g of 2,2,6,6-tetramethyl-4-(butylamino)piperidine [obtained as described in Preparation i(A)] and 2.77 g of sodium bicarbonate were heated under reflux in 20 ml of xylene for 29 hours. At the end of this time, the xylene was removed by distillation under reduced pressure, and a mixture of methylene chloride and water was added to the resulting residue, after which the mixture was shaken. The methylene chloride layer was separated, dried and concentrated by evaporation under reduced pressure, and the resulting residue was purified by silica gel column chromatography (using a 20:10:1:1 by volume mixture of hexane, diethyl ether, ethanol and triethylamine as eluent), to yield 5.46 g of the title compound melting at 40° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05486556
Quelldatensatzuspto-grants-1996_01
ORD IDord-4b2376a98a4048179b6e95cb7445ec51
Quellennotizuspto-grants-1996_01