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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258374Generated: October 26, 2026

Bromine → N-(3-bromo-4-hydroxynaphthalen-1-yl)thiophene-2-sulfonamide

https://huagongshe.com/reaction/1258374

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantN-(4-hydroxynaphthalen-1-yl)thiophene-2-sulfonamideHCID 697391—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductN-(3-bromo-4-hydroxynaphthalen-1-yl)thiophene-2-sulfonamideHCID 771854436.4%

Reaction Steps

305.7 mg N-(4-hydroxynaphthalen-1-yl)thiophene-2-sulfonamide (3) was dissolved in 1 ml DMF, to which at 0° C. was added 320 mg Br2 in 1 ml dichloromethylene solution. After stirred at r.t. for 1 h, 558 μl TEA was added at 0° C. The reaction was stirred at r.t. overnight and diluted with ethyl acetate to 50 ml. The organic phase was washed with water and brine. Dried over Na2SO4, the organic phase was filtered and concentrated. The crude product was purified via flash chromatography (Hex/EtOAc gradient) affording an orange-red solid 140 mg (36.4%), m.p.: 128-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466157B2
Source datasetuspto-grants-2013_06
ORD IDord-e70a62bbf0c34ee1af8b0bb449b5cebd
Source noteuspto-grants-2013_06