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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2180402Generated: October 29, 2026

2-Methoxyaniline → HCID 67019533, compound

https://huagongshe.com/reaction/2180402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MethoxyanilineHCID 7000—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(3-Chlorosulfonylphenyl)acrylic acid methyl esterHCID 73708742—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67019533HCID 6701953379%

Reaction Steps

A solution of 3-(3-chlorosulfonylphenyl)acrylic acid methyl ester (3) (0.40 g, 1.53 mmol) in dioxane (5 ml) was added to a mixture of o-anisidine (0.19 g, 1.54 mmol) in dioxane (1 ml) and NaHCO3 (0.26 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 water. 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 (0.42 g, 79%) as a white solid. 1H NMR (DMSOd-6, HMDSO), δ: 3.43 (3H, s); 3.72 (3H, s); 6.60 (1H, d, J=16.0 Hz); 6.72-7.27 (4H, m); 7.45-8.12 (5H, m); 9.47 (1H, s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06888027B2
Source datasetuspto-grants-2005_05
ORD IDord-40cfe6d8f8af4feb9d33e0e2e8ee4233
Source noteuspto-grants-2005_05