Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1297168Generated: November 2, 2026

N-bromobutanimide → 5-Bromo-4-methoxythiophene-2-sulfonamide

https://huagongshe.com/reaction/1297168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 15669338HCID 15669338—
SolventDichloromethaneHCID 6344—
Product5-Bromo-4-methoxythiophene-2-sulfonamideHCID 2201952982.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 4-methoxythiophene-2-sulfonamide (240 mg, 1.24 mmol) in CH2Cl2 (40 mL) is added N-bromosuccinimide (287 mg, 1.61 mmol). The reaction mixture is stirred at 0° C. for 7 hr. After 7 hr, the reaction mixture is diluted with CH2Cl2 (150 mL). The organic layer is washed with brine then dried (Na2SO4), filtered and concentrated in vacuo. The crude product is chromatographed on silica gel, eluting with Hex:EtOAc (2:1) to afford the title compound (277 mg, 82%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07250430B2
Source datasetuspto-grants-2007_07
ORD IDord-fc39981fd2ac4903b40fa8d59f58fa2d
Source noteuspto-grants-2007_07