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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258369Generated: November 3, 2026

4-Nitrobenzenesulfonyl chloride → 2-Thiophenesulfonamide

https://huagongshe.com/reaction/1258369

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
Reactant2-ThiophenesulfonamideHCID 72881—
Product4-NitrobenzenesulfonamideHCID 22784—
Product2-ThiophenesulfonamideHCID 7288196.6%

Reaction Steps

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). HRMS (ESI-ve) m/z calculated for C6H6N2O4S (M−H)− 200.9976. Found 200.9986.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08466157B2
Source datasetuspto-grants-2013_06
ORD IDord-3b11d11450674294b59702368e9ed290
Source noteuspto-grants-2013_06