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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630331Generated: October 26, 2026

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

https://huagongshe.com/reaction/630331

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 numberUS09315509B2
Source datasetuspto-grants-2016_04
ORD IDord-551cde540ae246c48d2e5c371ea70662
Source noteuspto-grants-2016_04