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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2298808Generated: October 30, 2026

HCID 18378604, compound → HCID 18378582, compound

https://huagongshe.com/reaction/2298808

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18378604HCID 18378604—
ReactantPotassium tert-butoxideHCID 23665647—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductHCID 18378582HCID 1837858221.8%

Reaction Steps

To a solution of methyltriphenylphosphonium bromide (607 mg) in N,N-dimethylformamide (10 ml) was added potassium-tert-butoxide (191 mg), and the mixture was stirred at room temperature for 30 minutes. Methyl 2-methoxy-4-(2,3,4,5-tetrahydro-5-oxo-1H-1-benzazepin-1-yl)carbonylbenzoate (300 mg) was added to the resulting solution, and the mixture was stirred at room temperature overnight. The mixture was diluted with ethyl acetate and the solution was washed successively with 1N hydrochloric acid, water and brine. The organic layer was dried over magnesium sulfate and the solvent was evaporated in vacuo to give an oil. The crude product was purified by silica gel column chromatography (10% ethyl acetate in hexane) to give methyl 2-methoxy-4-(2,3,4,5-tetrahydro-5-methylene-1H-1-benzazepin-1-yl)carbonylbenzoate (65 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06495542B1
Source datasetuspto-grants-2002_12
ORD IDord-5b8a3695cbad4e34b66b2498c4c82f7e
Source noteuspto-grants-2002_12