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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351061Generated: October 31, 2026

2-Naphthylamine → 3-[3-(Naphthalen-2-ylsulfamoyl)-phenyl]-acrylic acid methyl ester

https://huagongshe.com/reaction/351061

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphthylamineHCID 7057—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(3-Chlorosulfonylphenyl)acrylic acid methyl esterHCID 73708742—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product3-[3-(Naphthalen-2-ylsulfamoyl)-phenyl]-acrylic acid methyl esterHCID 6701949637%

Reaction Steps

A solution of 3-(3-chlorosulfonylphenyl)acrylic acid methyl ester (3) (1.0 g, 3.83 mmol) in dioxane (10 ml) was added to a mixture of 2-aminonaphthalene (0.55 g, 3.83 mmol) and NaHCO3 (0.48 g, 5.71 mmol) in water (6 ml), and the resultant solution was stirred at room temperature until the completion of the reaction (control by TLC). 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 petroleum ether-ethyl acetate (3:2, v/v) as eluent. The obtained product was crystallised from petroleum ether-ethyl acetate to give the title compound (0.52 g, 34%) as a white solid. 1H NMR (DMSO-d6, HMDSO), 6:3.73 (3H, s); 6.67 (1H, d, J=16.0 Hz); 7.21–8.07 (11H, m); 8.16 (1H, s); 10.55 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183298B2
Source datasetuspto-grants-2007_02
ORD IDord-4f656cc6e3e647c0b90f3a9f34103541
Source noteuspto-grants-2007_02