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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186653Generated: November 2, 2026

4-Nitrobenzenesulfonyl chloride → 4-Nitrobenzenesulfonamide

https://huagongshe.com/reaction/1186653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
Reactant2-ThiophenesulfonamideHCID 72881—
Product4-NitrobenzenesulfonamideHCID 22784—

Reaction Steps

5.2.2 4-nitrobenzenesulfonamide was prepared according to the procedure for thiophene-2-sulfonamide YG1-030 except using 4-nitrobenzenesulfonyl chloride, which afforded the title compound 1.953 g (96.6%) as a pale yellow solid, m.p.: 178-180° C. 1H-NMR, 400 MHz, d6-DMSO, δ (ppm): 8.40 (d, J=8.6 Hz, 2H), 8.04 (d, J=8.6 Hz, 2H), 7.72 (br, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673910B2
Source datasetuspto-grants-2014_03
ORD IDord-eff7b14dbbce4317875789ea72920cb2
Source noteuspto-grants-2014_03