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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099992Generated: October 25, 2026

Tetrahydrofuran → HCID 57796874, compound

https://huagongshe.com/reaction/2099992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantSodium BicarbonateHCID 516892—
Reactant3-(2H-1,3-Benzodioxol-5-yl)prop-2-enoyl chlorideHCID 53411279—
ReactantHCID 57495369HCID 57495369—
SolventWaterHCID 962—
ProductHCID 57796874HCID 5779687471%

Reaction Steps

(Method G3) A solution of 3-benzo[1,3]dioxol-5-yl-acryloyl chloride (2a) (0.41 g, 1.95 mmol) in tetrahydrofuran (8.0 ml) was added to a mixture of m-aminophenylacrylic acid methyl ester (0.35 g, 1.97 mmol) in tetrahydrofuran (12.0 ml) and NaHCO3 (0.25 g, 3.00 mmol) in water (7.0 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 dichlormethane-methanol (40:1, v/v) as eluent. The obtained product was washed with diethyl ether to give the title compound (0.50 g, 71%). 1H NMR (DMSO-d6, HMDSO), δ: 3.73 (3H, s); 6.09 (2H, s); 6.49 (1H, d, J=16.0 Hz); 6.67 (1H, d, J=16.0 Hz); 6.89-7.83 (8H, m); 7.98 (1H, br s); 10.23 ppm (1H, br s)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569724B2
Source datasetuspto-grants-2009_08
ORD IDord-b56335c76cf249609ff9f72dc109b2fc
Source noteuspto-grants-2009_08