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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-aminobenzoate | HCID 6877 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Furylacrylic acid | HCID 10876 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 2-[3-(2-furyl)acrylamido]benzoate | HCID 4450927 | 30.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05006548 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-9cb8dfb2cb994905a60b3a6f3c499400 |
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| Source note | uspto-grants-1991_04 |
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