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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53849Generated: October 24, 2026

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

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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-(Hexyloxy)benzoic acidHCID 70834—
ReactantP,P-Diphenylphosphinic azideHCID 199401—
Reactant4-(2-Aminophenethyl)-2,6-di-tert-butylphenolHCID 19960469—
SolventTolueneHCID 1140—
ProductN-[2-(3,5-di-tert-butyl-4-hydroxyphenethyl)phenyl]-N'-(4-hexyloxyphenyl)ureaHCID 1996059171.1%

Reaction Conditions

Temperature90 °C

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05621010
Source datasetuspto-grants-1997_04
ORD IDord-5c141c9bdd984689b832fcc33d073f7a
Source noteuspto-grants-1997_04