HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 840965Generated: October 30, 2026
Hydrochloric Acid → Ethyl 1,2,3,4-tetrahydro-5-oxo-benz[b]oxepine-4-carboxylate
https://huagongshe.com/reaction/840965
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 15486834 | HCID 15486834 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | Ethyl 1,2,3,4-tetrahydro-5-oxo-benz[b]oxepine-4-carboxylate | HCID 15486835 | 83.3% |
Reaction Steps
A mixture of ethyl 4-(2-ethoxycarbonylphenyloxy)-butyrate (13.0 g, 46.4 mmol), 60% sodium hydride (5.56 g, 139 mmol), ethanol (2.5 ml) and toluene (250 ml) was stirred at 80-85° C. for 2 hours. The reaction mixture was poured into cold 1N hydrochloric acid and extracted twice with ethyl acetate, and the extract solution was washed with a 5% aqueous sodium chloride solution and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by a silica gel column chromatography (eluent; ethyl acetate:n-hexane=3:97) to obtain 9.05 g of ethyl 1,2,3,4-tetrahydro-5-oxo-benz[b]oxepine-4-carboxylate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06369110B1 |
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| Source dataset | uspto-grants-2002_04 |
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| ORD ID | ord-7489b2e3395446a59c8f89f525cdea19 |
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| Source note | uspto-grants-2002_04 |
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