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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1409007Generated: October 31, 2026

N-bromobutanimide → HCID 59446608, compound

https://huagongshe.com/reaction/1409007

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 66743233HCID 66743233—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59446608HCID 5944660895.3%

Reaction Conditions

Temperature50 °C

Reaction Steps

1-Bromopyrrolidine-2,5-dione (20.8 g) was added to a stirring solution (300 mL) of 5-ethyl-N,N-dimethyl-1H-pyrazole-1-sulfonamide (19.8 g) in tetrahydrofuran at room temperature. The reaction system was heated to 50° C., stirred for 2 hr and concentrated under reduced pressure. The residue was poured into saturated aqueous sodium hydrogen carbonate, and the mixture was extracted with ethyl acetate, and dried over anhydrous magnesium sulfate. Insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate/hexane) to give the title compound (26.2 g) as a yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921354B2
Source datasetuspto-grants-2014_12
ORD IDord-577b4a5eb1434f3f8a43fbf67f428737
Source noteuspto-grants-2014_12