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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1084822Erstellt: 26. Oktober 2026

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

https://huagongshe.com/reaction/1084822

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl 2-aminobenzoateHCID 6877—
EduktTriethylamineHCID 8471—
EduktFurylacrylic acidHCID 10876—
Edukt2-Chloro-1-methylpyridinium iodideHCID 167069—
LösungsmittelDichloromethaneHCID 6344—
ProduktEthyl 2-[3-(2-furyl)acrylamido]benzoateHCID 445092730,2%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05006548
Quelldatensatzuspto-grants-1991_04
ORD IDord-9cb8dfb2cb994905a60b3a6f3c499400
Quellennotizuspto-grants-1991_04