Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949147Generated: October 30, 2026

Sulfuric Acid → Methyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetate

https://huagongshe.com/reaction/1949147

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfuric AcidHCID 1118—
ReactantMethyl vinyl ketoneHCID 6570—
ReactantTriethylamineHCID 8471—
ReactantHCID 86677616HCID 86677616—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductMethyl 2-(3,4-dichlorophenyl)-2-(3-oxobutylthio)acetateHCID 5828151976%

Reaction Conditions

Temperature60 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399685B2
Source datasetuspto-grants-2013_03
ORD IDord-3dfcbd01f2134e3685e314a14f312a29
Source noteuspto-grants-2013_03