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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantEthanolHCID 702—
ReactantSodium hydrideHCID 24758—
ReactantHCID 15486834HCID 15486834—
SolventTolueneHCID 1140—
ProductEthyl 1,2,3,4-tetrahydro-5-oxo-benz[b]oxepine-4-carboxylateHCID 1548683583.3%

Reaction Conditions

Temperature82.5 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06369110B1
Source datasetuspto-grants-2002_04
ORD IDord-7489b2e3395446a59c8f89f525cdea19
Source noteuspto-grants-2002_04