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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351041Generated: October 30, 2026

3-Methoxyaniline → HCID 67019550, compound

https://huagongshe.com/reaction/351041

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxyanilineHCID 10824—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(3-Chlorosulfonylphenyl)acrylic acid methyl esterHCID 73708742—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67019550HCID 6701955082.8%

Reaction Steps

A solution of 3-(3-chlorosulfonylphenyl)-acrylic acid methyl ester (3) (0.4 g, 1.53 mmol) in dioxane (5 ml) was added to a mixture of 3-methoxyphenylamine (0.189 g, 1.53 mmol) in dioxane (1 ml) and NaHCO3 (0.25 g, 3.06 mmol) in water (3 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 (2:1, v/v) as eluent. The obtained product was washed with diethyl ether to give the title compound (0.44 g, 82%) as a white solid. 1H NMR (DMSO-d6, HMDSO), δ: 3.60 (3H, s), 3.71 (3H, s); 6.52–6.74 (3H, m); 6.63 (1H, d, J=16.0 Hz); 7.07 (1H, m); 7.43–8.05 (5H, m); 10.27 ppm (1H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07183298B2
Source datasetuspto-grants-2007_02
ORD IDord-bf760dff423d44a5a4464beb10ac62f5
Source noteuspto-grants-2007_02