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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 343603Generated: October 25, 2026

Triethylamine → 1-Ethyl-3-(2-ethyl-6-isopropylphenyl)-2-thioxo-imidazolin-4-one

https://huagongshe.com/reaction/343603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Ethyl-6-isopropylphenyl isothiocyanateHCID 144234—
ReactantN-EthylglycineHCID 316542—
SolventChloroformHCID 6212—
Product1-Ethyl-3-(2-ethyl-6-isopropylphenyl)-2-thioxo-imidazolin-4-oneHCID 11185387—

Reaction Steps

A mixture of the crude N-ethyl glycine (18.4 g), 2-ethyl-6-isopropylphenyl-isothiocyanate, (20.5 g), triethyl amine (20.2 g) and chloroform (300 mL) was heated at reflux for 6 hours. The solvent was evaporated. The residue was dissolved in ethyl acetate (500 mL) and washed with water (500 mL). The organic phase was evaporated to dryness. The residue was dissolved in ethanol (50 mL), then diluted with diethyl ether (200 mL). The solution was saturated with hydrogen chloride. The mixture was filtered. The solid was discarded. The filtrate was evaporated to dryness. Purification was achieved by flash chromatography on silica gel (5-10% ethyl acetate in hexane). Crystallization from diethyl ether/hexane afforded pure title compound (7.5 g) as a white solid, m.p. 77°-79° C. Anal. Calcd. for. C16H22N2OS: C, 66.17; H, 7.64; N, 9.65. Found: C, 66.12; H, 7.77; N, 9.69. Mass spectrum (EI, M.+) m/z 290.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05861517
Source datasetuspto-grants-1999_01
ORD IDord-1d5a56b47b9343c49c3780fb7af10a54
Source noteuspto-grants-1999_01