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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1166603Generated: November 4, 2026

Ethyl Acetate → HCID 22998966, compound

https://huagongshe.com/reaction/1166603

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantAmmonium ChlorideHCID 25517—
ReactantHCID 9813533HCID 9813533—
ReactantHCID 178418244HCID 178418244—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22998966HCID 22998966—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of methyltriphenylphosphonium bromide (2.2 g) in THF (20 ml) was added 1.6M n-butyl lithium hexane solution (2.9 ml) at 0° C. for 30 minutes. To the reaction mixture cooled to 0° C. was added 5,11-dihydro-7-methoxypyrido[2,3-c][1]benzoxepin-5-one (1.0 g) dropwise as THF solution (5 ml), and the mixture was warmed to room temperature, and stirred for 3 hours. Aqueous ammonium chloride and ethyl acetate were added to the reaction mixture, the organic layer was separated and washed with saturated aqueous sodium chloride, and dried with magnesium sulfate. The solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography eluting with ethyl acetate-hexane (1:4) to give 5,11-dihydro-7-methoxy-5-methylenepyrido[2,3-c][1]benzoxepine (0.14 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06613905B1
Source datasetuspto-grants-2003_09
ORD IDord-c13fb0c167a84bf7a58cbfc4eb4c89ea
Source noteuspto-grants-2003_09