HuagongsheHuagongshe Chemistry Print Report · For research reference only
3,4-Diethoxybenzene-1-carbothioamide → HCID 68711915, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3,4-Diethoxybenzene-1-carbothioamide | HCID 7745250 | — |
| Reactant | HCID 86618358 | HCID 86618358 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 68711915 | HCID 68711915 | 112.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07655680B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-89312107e36d4804a7991b105df744c6 |
| Source note | uspto-grants-2010_02 |