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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097557Generated: November 1, 2026

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

https://huagongshe.com/reaction/2097557

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 numberUS08450352B2
Source datasetuspto-grants-2013_05
ORD IDord-715a81a7b219420799e4b3c257a507f9
Source noteuspto-grants-2013_05