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HRID 53849Erstellt: 23. Oktober 2026

Triethylamine → N-[2-(3,5-di-tert-butyl-4-hydroxyphenethyl)phenyl]-N'-(4-hexyloxyphenyl)urea

https://huagongshe.com/de/reaction/53849

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4-(Hexyloxy)benzoic acidHCID 70834—
EduktP,P-Diphenylphosphinic azideHCID 199401—
Edukt4-(2-Aminophenethyl)-2,6-di-tert-butylphenolHCID 19960469—
LösungsmittelTolueneHCID 1140—
ProduktN-[2-(3,5-di-tert-butyl-4-hydroxyphenethyl)phenyl]-N'-(4-hexyloxyphenyl)ureaHCID 1996059171,1%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A solution of diphenylphosphorylazide (0.93 g, 3.4 mmol), 4-hexyloxybenzoic acid (0.68 g, 3.1 mmol) and triethylamine (0.34 g, 3.4 mmol) in toluene (10 ml) was stirred at room temperature for 3.5 hrs and heated at about 90° C. for 2 hrs with stirring. After allowing the mixture to cool (under 0° C.), a solution of 4-(2-aminophenethyl)-2,6-di-tert-butylphenol (1.0 g, 3.1 mmol) in toluene (4 ml) was added dropwise. The solution was warmed up to room temperature and stirred overnight. After distilling off the solvent and purification of the residue by a silica gel column chromatography, recrystallization from ethyl acetate/hexane afforded N-[2-(3,5-di-tert-butyl-4-hydroxyphenethyl)phenyl]-N'-(4-hexyloxyphenyl)urea (1.2 g, 71% yield). m.p. 174°-176° C.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05621010
Quelldatensatzuspto-grants-1997_04
ORD IDord-5c141c9bdd984689b832fcc33d073f7a
Quellennotizuspto-grants-1997_04