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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2237653Generated: October 30, 2026

Hydrochloric Acid → N-(5-fluoro-2-nitrophenyl)benzenesulfonamide

https://huagongshe.com/reaction/2237653

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantBenzenesulfonamideHCID 7370—
ReactantSodium hydrideHCID 24758—
Reactant2,4-DifluoronitrobenzeneHCID 67967—
SolventDimethylformamideHCID 6228—
ProductN-(5-fluoro-2-nitrophenyl)benzenesulfonamideHCID 2227257370.3%

Reaction Steps

Benzenesulfonamide (3.14 g, 20 mmol) was dissolved in DMF (100 mL) and NaH (60% in oil, 40 mmol, 1.60 g) was added. The reaction was stirred until the gas evolution ceased. 2,4-Difluoronitrobenzene (18 mmol, 2.9 g, 2 mL) was added and the reaction mixture was stirred over night at 35° C. The reaction mixture was poured into HCl (1M aq, 100 mL) and extracted with toluene (25 mL×5). The organic phase was dried (MgSO4) and concentrated and re-crystallized from EtOH to give a first crop of 3.75 g of a yellow solid. A second crop of 0.20 g was collected from the EtOH remains. Yield 3.95 g, 13.3 mmol (74%). MS (posES-FIA) m/z=found: 296; Calc: 296,0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07718650B2
Source datasetuspto-grants-2010_05
ORD IDord-069c887987784f9a82440fdb9280bffe
Source noteuspto-grants-2010_05