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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 16498생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/16498

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Aminoacetaldehyde dimethyl acetalHCID 89728—
반응물p-Acetoxybenzoyl chlorideHCID 2756254—
용매DichloromethaneHCID 6344—
생성물4-(2,2-Dimethoxyethylcarbamoyl)phenyl acetateHCID 1174755581.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737145B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-9aecc64b4b81414099ed3b819d3c482e
출처 메모uspto-grants-2010_06