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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1754115Generated: November 1, 2026

4-Nitrobenzenesulfonyl chloride → HCID 27301538, compound

https://huagongshe.com/reaction/1754115

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Nitrobenzenesulfonyl chlorideHCID 7404—
Reactant2-(Trifluoromethoxy)anilineHCID 73754—
SolventPyridineHCID 1049—
ProductHCID 27301538HCID 2730153876.6%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a pre-cooled solution of 2-(trifluoromethoxy)aniline (1.8 g, 10.16 mmol) in pyridine (20 ml) was added 4-nitrobenzene-1-sulfonyl chloride (2.252 g, 10.16 mmol) in 5-10 mL of pyridine at 0° C. slowly. The reaction mixture was stirred and heated to 85° C. for 3 h, then cooled down to 45° C. and stirred at the same temperature over weekend. The solvent was removed under reduced pressure. The residue was diluted with methylene chloride and washed with 1N HCl (×2), water (×2), and brine. The organic layer was separated, dried with anhydrous Na2SO4, filtered and concentrated under reduced pressure to give 2.82 g of title product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09169209B2
Source datasetuspto-grants-2015_10
ORD IDord-1d27b79954944e76b47e122f20afdc49
Source noteuspto-grants-2015_10