戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 53849作成日:2026年10月23日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-(Hexyloxy)benzoic acidHCID 70834—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物4-(2-Aminophenethyl)-2,6-di-tert-butylphenolHCID 19960469—
溶媒TolueneHCID 1140—
生成物N-[2-(3,5-di-tert-butyl-4-hydroxyphenethyl)phenyl]-N'-(4-hexyloxyphenyl)ureaHCID 1996059171.1%

反応条件

温度90 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05621010
出典データセットuspto-grants-1997_04
ORD IDord-5c141c9bdd984689b832fcc33d073f7a
出典メモuspto-grants-1997_04