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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192887Generated: October 26, 2026

Water → Ethyl [3-bromo-4-(cyclopropylsulfanyl)phenyl](oxo)acetate

https://huagongshe.com/reaction/2192887

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthoxalyl chlorideHCID 20884—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant1-Bromo-2-(cyclopropylsulfanyl)benzeneHCID 59570916—
SolventDichloromethaneHCID 6344—
ProductEthyl [3-bromo-4-(cyclopropylsulfanyl)phenyl](oxo)acetateHCID 5957089842.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of aluminum chloride (40.2 g) in dichloromethane (1200 mL) was added dropwise ethyl chloro(oxo)acetate (32.3 g) at 0° C., followed by stirring at the same temperature for 1 hour. To the reaction mixture was added dropwise a solution of 1-bromo-2-(cyclopropylsulfanyl)benzene (49.3 g) in dichloromethane (280 mL) while keeping it at 5° C. or lower, followed by stirring at room temperature for 1 hour. The reaction mixture was cooled to 0° C., and water was added thereto to stop the reaction. The reaction mixture was extracted with ethyl acetate and the organic layer was sequentially washed with water, a saturated aqueous sodium hydrogen carbonate solution, and saturated brine. The solution was dried over anhydrous magnesium sulfate and then concentrated. The residue was purified by silica gel chromatography to obtain ethyl[3-bromo-4-(cyclopropylsulfanyl)phenyl](oxo)acetate (29.8 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329707B2
Source datasetuspto-grants-2012_12
ORD IDord-984d21cb8921458497f5da18cbbad558
Source noteuspto-grants-2012_12