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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325037Generated: October 26, 2026

Benzenesulfonyl chloride → N-{5-[2-(4-Cyanophenyl)ethoxy]-2-methylphenyl}benzenesulfonamide

https://huagongshe.com/reaction/325037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium BicarbonateHCID 516892—
ReactantAmino-5-[2-(4-cyanophenyl)ethoxy]-2-methylbenzeneHCID 22033532—
SolventPyridineHCID 1049—
ProductN-{5-[2-(4-Cyanophenyl)ethoxy]-2-methylphenyl}benzenesulfonamideHCID 22033468100%

Reaction Steps

Benzenesulfonyl chloride (22 μL; 0.17 mmol) was added to a cold solution (ice :water temperature) of amino-5-[2-(4-cyanophenyl)ethoxy]-2-methyl-benzene (0.041 g; 0.16 mmol; from step (ii) above) in pyridine (4 mL) The reaction flask was left overnight in a refrigerator. NaHCO3/aq (sat.) was added and the solution extracted twice with EtOAc. The combined organic phases were washed with water, HCl/aq (2M) and water. Drying (MgSO4) and evaporation of the solvent in vacuo afforded 0.062 g (100%) of the sub-title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06221898B1
Source datasetuspto-grants-2001_04
ORD IDord-e7be5e1600be4462aba977e363e80d52
Source noteuspto-grants-2001_04