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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1362550Generated: October 26, 2026

Tetrahydrofuran → HCID 66958338, compound

https://huagongshe.com/reaction/1362550

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant3-Phenylprop-2-enoyl chlorideHCID 66023—
ReactantSodium BicarbonateHCID 516892—
Reactantm-Aminophenylacrylic acid methyl esterHCID 57495369—
SolventWaterHCID 962—
ProductHCID 66958338HCID 6695833870%

Reaction Steps

A solution of phenylacryloylchloride (0.47 g, 2.85 mmol) (Acros) in tetrahydrofuran (10.0 ml) was added to a mixture of m-aminophenylacrylic acid methyl ester (7) (0.44 g, 2.50 mmol) in tetrahydrofuran (15.0 ml) and NaHCO3 (0.37 g, 4.50 mmol) in water (8.0 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 petroleum ether-ethyl acetate (2:1, v/v) as eluent. The obtained product was washed with diethyl ether to give the title compound (0.54 g, 70%). 1H NMR (DMSO-d6, HMDSO), δ: 3.72 (3H, s); 6.52 (1H, d, J=16.0 Hz); 6.83 (1H, d, J=16.0 Hz); 7.29-7.85 (10H, m); 7.98 (1H, br s); 10.32 (1H, br s).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880020B2
Source datasetuspto-grants-2011_02
ORD IDord-ecbd7d21b4784336a04129beb2b8488d
Source noteuspto-grants-2011_02