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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1441708Generated: November 1, 2026

3,4-Diethoxybenzene-1-carbothioamide → HCID 68711915, compound

https://huagongshe.com/reaction/1441708

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4-Diethoxybenzene-1-carbothioamideHCID 7745250—
ReactantHCID 86618358HCID 86618358—
SolventEthanolHCID 702—
ProductHCID 68711915HCID 68711915112.6%

Reaction Steps

3,4-diethoxythiobenzamide (0.63 g, 2.8 mmol) was added to a solution (20 ml) of ethyl 2-benzoyl-5-bromo-4-oxopentanoate (0.90 g, 2.8 mmol) in ethanol, followed by heating under reflux for 1.5 hours. After cooling to room temperature, the solvent was distilled off under reduced pressure, and the residue was subjected to extraction with ethyl acetate. The organic layer was washed with a saturated aqueous sodium hydrogencarbonate solution and a saturated salt solution, and dried over anhydrous sodium sulfate. The solvent was distilled off under reduced pressure, to thereby obtain 1.43 g (yield: 65%) of ethyl 2-[2-(3,4-diethoxyphenyl)thiazole-4-ylmethyl]-3-oxo-3-phenylpropionate as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07655680B2
Source datasetuspto-grants-2010_02
ORD IDord-89312107e36d4804a7991b105df744c6
Source noteuspto-grants-2010_02