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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2079603Generated: October 25, 2026

Citric Acid → N-(4-Chlorophenyl)-3-methoxy-benzenesulfonamide

https://huagongshe.com/reaction/2079603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantPyridineHCID 1049—
Reactant4-ChloroanilineHCID 7812—
Reactant3-Methoxybenzenesulfonyl chlorideHCID 2737504—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(4-Chlorophenyl)-3-methoxy-benzenesulfonamideHCID 57788151—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 4-chloroaniline (400 mg, 3.13 mmol) in anhydrous dichloromethane (40 mL) were added 3-methoxybenzenesulfonyl chloride (648 mg, 3.13 mmol) followed by pyridine (297.2 mg, 3.76 mmol). The mixture was allowed to stir for 12 h at 25° C. 10% citric acid solution (20 mL) and water (20 mL) was added. The organic phase was dried (Na2SO4), and evaporated under reduced pressure yielding the title compound as solid which was used as such in the next step. Yield: 900 mg (96%). MS (m/e): 296 (M+−H); 1H-NMR (CDCl3, 400 MHz): δ 3.76 (s, 3H), 6.48 (brs, 1H), 7.0 (d, J=8.72 Hz, 2H), 7.06 (d, J=7.76 Hz, 1H), 7.21 (m, 3H), 7.32 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07932269B2
Source datasetuspto-grants-2011_04
ORD IDord-bf36f5f2bdfa42f99f69fd1332a065ac
Source noteuspto-grants-2011_04