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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1804063Generated: October 31, 2026

Dichloromethane → Methyl 4-bromo-2-(1,1-dioxoisothiazolidin-2-yl)benzoate

https://huagongshe.com/reaction/1804063

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantTriethylamineHCID 8471—
Reactant3-Chloropropanesulphonyl chlorideHCID 15410—
ReactantMethyl 2-Amino-4-bromobenzoateHCID 17871390—
SolventWaterHCID 962—
ProductMethyl 4-bromo-2-(1,1-dioxoisothiazolidin-2-yl)benzoateHCID 58484624—

Reaction Steps

To a mixture of methyl 2-amino-4-bromobenzoate (5 g), triethylamine (5.73 mL), methylene chloride (39 mL) was added 3-chloropropanesulfonyl chloride (3.44 mL) under ice-cooling, and the mixture was stirred at room temperature. Water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with diluted hydrochloric acid and saturated brine, and the solvent was evaporated. To the residue were added 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU) (3.9 mL) and DMF (29 mL), and the mixture was stirred at room temperature. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with diluted hydrochloric acid and saturated brine, and the solvent was evaporated. To the residue was added isopropyl ether, and the precipitated solid was collected by filtration to give the title compound (5.045 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08354401B2
Source datasetuspto-grants-2013_01
ORD IDord-d9f004fcb7054bffbb543cbfdd147709
Source noteuspto-grants-2013_01