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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2104095Generated: October 30, 2026

Water → 2-(2-Ethoxycarbonyl-acetylamino)-4-phenyl-thiophene-3-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2104095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantEthyl 2-amino-4-phenylthiophene-3-carboxylateHCID 73242—
Reactant2-Ethylpropanedioyl dichlorideHCID 10920924—
SolventDichloromethaneHCID 6344—
Product2-(2-Ethoxycarbonyl-acetylamino)-4-phenyl-thiophene-3-carboxylic acid ethyl esterHCID 68432262—

Reaction Conditions

Temperature0 °C

Reaction Steps

2-Amino-4-phenyl-thiophene-3-carboxylic acid ethyl ester (5.0 g, 0.02 M) was dissolved in anhydrous dichloromethane (150 ml). Triethylamine (5.56 ml, 0.04 M) was added and the mixture cooled to 0° C. Ethyl Malonyl Chloride (3.79 ml, 0.03 M) was added over 5 min maintaining the temperature at 0° C. The reaction was then stirred at room temperature for 1 hr. Water (100 ml) was added and the organic layer separated. The aqueous layer was extracted with a further 100 ml of dichloromethane. The organics were combined, washed with water (2×100 ml) and dried over sodium sulphate. The concentrated residues were columned on silica, eluting with ethylacetate-cyclohexane 5-10% v/v. Pure fractions were combined and concentrated and the residues triturated with hexane, decanted and dried to give 2-(2-ethoxycarbonyl-acetylamino)-4-phenyl-thiophene-3-carboxylic acid ethyl ester as a white solid. Yield=6.95 g (96.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07576212B2
Source datasetuspto-grants-2009_08
ORD IDord-0902940c1bd64d59be97ad0e10e11d8e
Source noteuspto-grants-2009_08