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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084822Generated: October 25, 2026

Ethyl 2-aminobenzoate → Ethyl 2-[3-(2-furyl)acrylamido]benzoate

https://huagongshe.com/reaction/1084822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 2-aminobenzoateHCID 6877—
ReactantTriethylamineHCID 8471—
ReactantFurylacrylic acidHCID 10876—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
SolventDichloromethaneHCID 6344—
ProductEthyl 2-[3-(2-furyl)acrylamido]benzoateHCID 445092730.2%

Reaction Steps

Under nitrogen stream, 2-chloro-1-methylpyridinium iodide (1.272 g, 4.34 mmol) was suspended in dry methylene chloride (5 ml). To the suspension a solution of 3-(2-furyl)acrylic acid (500 mg, 3.62 mmol), triethylamine (1.2 ml, 8.69 mmol), and ethyl 2-aminobenzoate (0.53 ml, 3.62 mmol) in dry methylene chloride (5 ml) was added. The mixture was heated under reflux for 40 hours. Then, the reaction mixture was diluted with methylene chloride, and washed with 10% aqueous HCl, saturated aqueous sodium chloride, 1N-aqueous NaOH, and saturated aqueous sodium chloride successively, and dried. Removal of solvent gave a viscous oil, which, on washing with n-hexane gave white solids of the title compound (312 mg, yield: 30.2%), which was recrystallized from methanol. m.p., 85°-86° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05006548
Source datasetuspto-grants-1991_04
ORD IDord-9cb8dfb2cb994905a60b3a6f3c499400
Source noteuspto-grants-1991_04