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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106782Generated: October 26, 2026

Allyl bromide → N-allyl-N-(2-bromo-5-nitrophenyl)methanesulfonamide

https://huagongshe.com/reaction/1106782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantCesium carbonateHCID 10796—
ReactantN-(2-bromo-5-nitrophenyl)methanesulfonamideHCID 18789758—
SolventMethyl Ethyl KetoneHCID 6569—
ProductN-allyl-N-(2-bromo-5-nitrophenyl)methanesulfonamideHCID 1878966799.8%

Reaction Steps

Allyl bromide (1.36 g, 11.25 mmol) was added to a mixture of N-(2-bromo-5-nitrophenyl)methanesulfonamide (1.66 g, 5.62 mmol) and cesium carbonate (5.49 g, 16.86 mmol) in methylethylketone (20 ml). The mixture was heated to reflux for 2 hr. The mixture was cooled and poured onto water. The product was extracted into ethyl acetate (2×75 ml) and the extracts were dried (anhydrous MgSO4) and concentrated to provide 1.88 g of N-allyl-N-(2-bromo-5-nitrophenyl)methanesulfonamide which required no purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057349
Source datasetuspto-grants-2000_05
ORD IDord-235f60488fa84068b962be97152430ff
Source noteuspto-grants-2000_05