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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 16498Generated: October 26, 2026

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

https://huagongshe.com/reaction/16498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAminoacetaldehyde dimethyl acetalHCID 89728—
Reactantp-Acetoxybenzoyl chlorideHCID 2756254—
SolventDichloromethaneHCID 6344—
Product4-(2,2-Dimethoxyethylcarbamoyl)phenyl acetateHCID 1174755581.1%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07737145B2
Source datasetuspto-grants-2010_06
ORD IDord-9aecc64b4b81414099ed3b819d3c482e
Source noteuspto-grants-2010_06