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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2374413Generated: October 28, 2026

Water → 2-Benzylamino-5-nitro-benzenesulfonamide

https://huagongshe.com/reaction/2374413

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzylamineHCID 7504—
Reactant2-Chloro-5-nitrobenzenesulfonamideHCID 66784—
ReactantDiisopropylethylamineHCID 81531—
SolventAcetonitrileHCID 6342—
Product2-Benzylamino-5-nitro-benzenesulfonamideHCID 2485839783.4%

Reaction Conditions

Temperature55 °C

Reaction Steps

A solution of 2-chloro-5-nitro-benzenesulfonamide (20 g, 84.52 mmol) in acetonitrile (169 mL) was treated with benzylamine (13.85 mL, 126.78 mmol), diisopropyl ethylamine (29.44 mL, 169.04 mmol) and stirred for 16 h at 55° C. The reaction was cooled to 25° C., poured into water (1.0 L) then placed in an ice bath while stirring. After 4 h a precipitate was filtered off and washed with the mother liquor to afford the desired product, 2-benzylamino-5-nitro-benzenesulfonamide (21.65 g, 70.45 mmol, 83.3% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) 6:4.64 (2H, d, J=4.6 Hz), 6.81 (1H, d, J=9.4 Hz), 7.23-7.44 (6H, m), 7.77 (2H, bs), 8.11 (1H, dd, J1=9.4 Hz, J2=2.3 Hz), 8.49 (1H, d, J=3.1 Hz). LC-MS (ESI) calcd for C13H13N3O4S 307.06. found 308.2 [M+H+] (100%), 615.2 [2M+H+] (81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07462611B2
Source datasetuspto-grants-2008_12
ORD IDord-cc217dc232cb49fe8b8606081bd14a8e
Source noteuspto-grants-2008_12