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HRID 16498作成日:2026年10月25日

Triethylamine → 4-(2,2-Dimethoxyethylcarbamoyl)phenyl acetate

https://huagongshe.com/reaction/16498

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物Aminoacetaldehyde dimethyl acetalHCID 89728—
反応物p-Acetoxybenzoyl chlorideHCID 2756254—
溶媒DichloromethaneHCID 6344—
生成物4-(2,2-Dimethoxyethylcarbamoyl)phenyl acetateHCID 1174755581.1%

反応手順

A solution of 4-(chlorocarbonyl)phenyl acetate (110 g, 553.87 mmol) in CH2Cl2 (500 mL) was cooled in an ice bath and treated with triethylamine (115 mL, 830 mmol, 1.5 equiv.) and 2,2-dimethoxyethanamine (63.36 mL, 581.56 mmol, 1.05 equiv.). The reaction mixture was allowed to warm to ambient temperature and the reaction was followed by TLC (CH2Cl2). The reaction mixture was concentrated under reduced pressure, diluted with ethyl acetate and filtered. The filtrate was washed with water. The aqueous layer was extracted with ethyl acetate (2×). The combined organic layers were washed with water, dilute mono-potassium phosphate (pH=5.4, pH of solution about 7), water, and brine, dried, and concentrated to give 120 g (81% th.; 109% pract.) of 4-(2,2-dimethoxyethylcarbamoyl)phenyl acetate as a light brown waxy solid with no further purification; 1H NMR (CDCl3) δ 7.79 (d, 2H), 7.15 (d, 2H), 6.32 (br. t, 1H), 4.47 (t, 1H), 3.58 (d, 2H), 3.41 (s, 6H), 2.30 (s, 3H) ppm.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737145B2
出典データセットuspto-grants-2010_06
ORD IDord-9aecc64b4b81414099ed3b819d3c482e
出典メモuspto-grants-2010_06