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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921820Generated: October 30, 2026

N-bromobutanimide → 2-bromo-4H,5H,6H-thieno(2,3-c)pyrrol-6-one

https://huagongshe.com/reaction/1921820

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
Reactant4H,5H,6H-thieno[2,3-c]pyrrol-6-oneHCID 20542805—
SolventAcetonitrileHCID 6342—
Product2-bromo-4H,5H,6H-thieno(2,3-c)pyrrol-6-oneHCID 59023141—

Reaction Steps

4,5-Dihydro-thieno[2,3-c]pyrrol-6-one (0.365 g, 2.63 mmol) is dissolved in acetonitrile (10 mL), and NBS (0.47 g, 2.63 mmol) is slowly added at −10° C. The reaction mixture is stirred at room temperature overnight. The solvent is removed in vacuo and the residue taken-up in EtOAc and washed with 1M NaOH. The organic phase is dried over MgSO4, filtered and concentrated in vacuo. The crude is purified by silica gel column chromatography eluting with a 50:50 mixture and then 50:70 petroleum ether-EtOAc. The title compound is isolated (91.1 mg, 16%). HPLC (254 nm): Rt 2.55 min (70.3%), m/z 218/220 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173656B2
Source datasetuspto-grants-2012_05
ORD IDord-25f33f57b63b40c392bd8ad9b5d2e7da
Source noteuspto-grants-2012_05