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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411134Generated: November 2, 2026

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

https://huagongshe.com/reaction/2411134

Reaction equation

Participants

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

Reaction Steps

Methyl 2-amino-4-bromobenzoate (5 g) and triethylamine (5.73 mL) were dissolved in methylene chloride (39 mL), 3-chloropropane-1-sulfonyl chloride (3.44 mL) was added under ice-cooling, and the mixture was stirred at room temperature. After completion of the reaction, water was added to the reaction mixture, and the mixture was extracted with chloroform. The organic layer was washed with dilute hydrochloric acid and saturated brine, and the solvent was evaporated. To the obtained residue were added 1,8-diazabicyclo[5.4.0]undec-7-ene (DBU)(3.9 mL) and N,N-dimethylformamide (29 mL), and the mixture was stirred at room temperature. After completion of the reaction, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with dilute hydrochloric acid and saturated brine, and the solvent was evaporated. To the obtained residue was added diisopropyl ether, and the precipitate was collected by filtration to give the title compound (5.05 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08816079B2
Source datasetuspto-grants-2014_08
ORD IDord-4c6b463126d94799b9350cac284e9bda
Source noteuspto-grants-2014_08