Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180382Generated: October 30, 2026

p-Toluidine → 3-(3-p-Tolylsulfamoyl-phenyl)-acrylic acid methyl ester

https://huagongshe.com/reaction/2180382

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-ToluidineHCID 7813—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(3-Chlorosulfonylphenyl)acrylic acid methyl esterHCID 73708742—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-(3-p-Tolylsulfamoyl-phenyl)-acrylic acid methyl esterHCID 6701951179.3%

Reaction Steps

A solution of 3-(3-chlorosulfonylphenyl)-acrylic acid methyl ester (3) (2.0 g, 7.23 mmol) in dioxane (10 ml) was added to a mixture of 4methylaniline (0.77 g, 7.23 mmol) in dioxane (20 ml) and NaHCO3 (1.2 g, 14.5 mmol) in water (20 ml), and the resultant solution was stirred at room temperature for one hour. The reaction mixture was evaporated and the residue was partitioned between ethyl acetate and 2N HCl. The organic layer was washed successively with water, saturated NaCl, and dried (Na2SO4). The solvent was removed and the residue was chromatographed on silica gel with dichloromethane-ethyl acetate (20:1, v/v) as eluent. The obtained product was washed with diethyl ether to give the title compound (1.9 g, 79%). 1H NMR (DMSO-d6, HMDSO), δ: 2.16 (3H, s); 3.69 (3H, s); 6.65 (1H, d, J=16.0 Hz); 7.00 (4H, s); 7.49-8.11 (5H, m); 10.14 (1H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06888027B2
Source datasetuspto-grants-2005_05
ORD IDord-8a9f0b125edb4de8b51cc22f992dbdc1
Source noteuspto-grants-2005_05