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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192902Generated: October 26, 2026

Hydrochloric Acid → HCID 59571040, compound

https://huagongshe.com/reaction/2192902

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantEthyl [3-bromo-4-(cyclopropylsulfanyl)phenyl](oxo)acetateHCID 59570898—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 59571040HCID 5957104053.6%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of ethyl[3-bromo-4-(cyclopropylsulfanyl)phenyl](oxo)acetate (30 g) in toluene (60 mL) was heated to 50° C., and a 3 M aqueous sodium hydroxide solution (36 mL) was added thereto at an internal temperature of 60° C. or lower, followed by stirring at 50° C. for 1 hour. After leaving it to be cooled at room temperature, water (150 mL) and ethyl acetate (100 mL) were added to the reaction mixture. To the aqueous layer was added concentrated hydrochloric acid (12 mL) under ice-cooling, followed by extraction with ethyl acetate (100 mL×3). The organic layer was washed with saturated brine (100 mL) and dried over anhydrous magnesium sulfate, and the solvent was then evaporated under reduced pressure. The residue was sequentially washed with hexane/ethyl acetate (19/1, 200 mL) and diethyl ether/hexane (1/2, 200 mL) to obtain [3-bromo-4-(cyclopropylsulfanyl)phenyl](oxo)acetic acid (14.7 g) as a pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329707B2
Source datasetuspto-grants-2012_12
ORD IDord-29ab79ee9a85418c98246572707858c5
Source noteuspto-grants-2012_12