HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1084861Generated: November 2, 2026
Hydrochloric Acid → Ethyl 3-methyl-4-methoxy-7-benzoylbenzofuran-2-carboxylate
https://huagongshe.com/reaction/1084861
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | Ethyl 4-methoxy-3-methyl-2-benzofurancarboxylate | HCID 9497663 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | Ethyl 3-methyl-4-methoxy-7-benzoylbenzofuran-2-carboxylate | HCID 15124007 | — |
Reaction Steps
To a solution of ethyl 3-methyl-4-methoxybenzofuran-2-carboxylate (1.00 g, 4.27 mmol) and benzoyl chloride (1.80 g, 12.81 mmol) in 1,2-dichloroethane (12 mL) was added aluminum chloride (1.71 g, 12.81 mmol) in portions. The mixture was heated to reflux for 1.5 hours then allowed to cool and poured into 2N HCl (50 mL). The resulting mixture was extracted with methylene chloride (3×30 mL) and the combined extracts washed with saturated NaHCO3 (3×25 mL), dried (Na2SO4), and concentrated. The crude product was purified by preparative HPLC, using 25% ethyl acetate in hexane as eluant, to afford ethyl 3-methyl-4-methoxy-7-benzoylbenzofuran-2-carboxylate mp. 137°-139° C.; 1H NMR d 1.27 (2H, t, J=6 Hz), 2.67 (3H, s), 3.95 (3H, s), 4.28 (2H, q, J=6 Hz), 6.66 (1H, d, J=8 Hz), 7.44 (3H, m), 7.72 (3H, m).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05006549 |
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| Source dataset | uspto-grants-1991_04 |
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| ORD ID | ord-4f739b9da9064a2c999752a0d28c0d85 |
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| Source note | uspto-grants-1991_04 |
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