戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 650041作成日:2026年10月25日

Triethylamine → N-(5-Chloro-2-methoxyphenyl)-N'-(2-oxo-2-phenylethyl)urea

https://huagongshe.com/reaction/650041

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-Chloro-2-isocyanato-1-methoxybenzeneHCID 144009—
反応物Ethanone, 2-amino-1-phenyl-, hydrochloride (1:1)HCID 2723597—
溶媒TetrahydrofuranHCID 8028—
溶媒Ethyl AcetateHCID 8857—
生成物N-(5-Chloro-2-methoxyphenyl)-N'-(2-oxo-2-phenylethyl)ureaHCID 21714202—

反応条件

温度60 °C

反応手順

5-Chloro-2-methoxyphenylisocyanate (5.3 g, 29 mmol) was dissolved in THF (250 ml) under N2 and heated to 60° C. To this solution was added 2-aminoacetophenone-HCl (5 g, 29 mmol) followed by triethylamine (3.8 g, 30 mmol). After being stirred 1.5 h, the reaction mixture was diluted with ethyl acetate (2 vol) and washed with 1N HCl solution, saturated NaCO3 solution, and brine before being dried, MgSO4. Concentration gave a solid which was washed with diethylether 6 g (65%). mp 171-173° C.; IR(KBr, υ=cm−1) 3336, 1706, 1644, 1600, 1560, 1482, 1262, 1220, 1182, 1126; 1H NMR (300 MHz, CDCl3) δ 3.79 (3H, s), 4.84 (2H, d, J=4.3 Hz), 5.97 (1H, br.s), 6.71 (1H, d, J=8.7 Hz), 6.88 (1H, dd, J=8.7 Hz, 2.5 Hz), 7.97-8.00 (2H, m), 8.18 (1H, d, J=2.5 Hz); MS(DCl)m/z: 319(MH+); Anal. calcd. for C16H15ClN2O3: C, 60.29; H, 4.74; N, 8.79. Found: C, 60.17; H, 4.64; N, 8.70.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06271249B1
出典データセットuspto-grants-2001_08
ORD IDord-77c03cb0277b4a92bfb2164ced71049c
出典メモuspto-grants-2001_08