Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186663Generated: October 26, 2026

4-Chlorobenzenesulfonamide → 4-chloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)benzenesulfonamide

https://huagongshe.com/reaction/1186663

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorobenzenesulfonamideHCID 66824—
Reactant(NE)-N-(3-chloro-4-oxonaphthalen-1-ylidene)thiophene-2-sulfonamideHCID 22524852—
SolventTetrahydrofuranHCID 8028—
Product4-chloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)benzenesulfonamideHCID 1381625—

Reaction Steps

5.2.34 4-chloro-N-(3-chloro-4-oxonaphthalen-1(4H)-ylidene)benzenesulfonamide (12e) was prepared according to the procedure for 12a except using 4-chlorobenzenesulfonamide, TiCL4.2THF and THF as solvent which afforded the title compound 452.2 mg (61.8%) as a yellow solid, m.p.: 138-140° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673910B2
Source datasetuspto-grants-2014_03
ORD IDord-fdb8c2bae5844c8380372912501c6030
Source noteuspto-grants-2014_03