HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 239228Generated: October 29, 2026
Sulfuric Acid → Methyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetate
https://huagongshe.com/reaction/239228
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 86677616 | HCID 86677616 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Methyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetate | HCID 58281519 | 76% |
Reaction Steps
To a methanol (2 mL) solution of methyl 2-thioacetyl-2-(3,4-dichlorophenyl)acetate (0.50 g, 1.7 mmol), concentrated sulfuric acid (0.050 mL, 0.55 equivalent amount) was added, followed by stirring at 60° C. for 3 hours. After the reaction solution was cooled to room temperature, it was dropwise added to an ethyl acetate (2 mL) solution of methyl vinyl ketone (0.17 mL, 1.2 equivalent amounts) and triethylamine (0.36 mL, 1.5 equivalent amount) at room temperature. The reaction solution was mixed with ethyl acetate (1 mL), followed by liquid separation with a mixed liquid of water-saturated salt solution (1:1, (v/v)), and further, the organic layer was washed with a saturated ammonium chloride aqueous solution and a saturated salt solution and dried over anhydrous magnesium sulfate. The drying agent was removed by filtration, and the solvent was distilled off to give the desired product as a colorless oil (0.42 g, yield: 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08642786B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-f869c5b20fee461f9516fe5df6a824e3 |
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| Source note | uspto-grants-2014_02 |
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