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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1196984Generated: October 26, 2026

Tetrahydrofuran → Methyl 11-methylene-6,11-dihydrodibenz-[b,e]oxepin-2-carboxylate

https://huagongshe.com/reaction/1196984

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantMethyl 11-oxo-6,11-dihydrodibenzo[b,e]oxepine-2-carboxylateHCID 2769045—
CatalystMethyltriphenyliphosphonium bromideHCID 74505—
ProductMethyl 11-methylene-6,11-dihydrodibenz-[b,e]oxepin-2-carboxylateHCID 10106958—

Reaction Steps

In 100 ml of tetrahydrofuran is suspended 25 g of methyltriphenylphosphonium bromide and 40 ml of 1.6 N-n-butyl lithium helium hexane solution is dropwise added thereto under a nitrogen atmosphere and ice-cooling. After stirring the mixture under ice-cooling for 30 minutes, a solution obtained by dissolving 15 g of methyl 11-oxo-6,11-dihydrodibenz[b,e]oxepin-2-carboxylate in 250 ml of tetrahydrofuran is dropwise added thereto and the mixture is stirred at room temperature for two hours. The solvent is distilled away under reduced pressure and the residue is purified by column chromatography on silica gel (eluent: hexane:ethyl acetate=3:1) to obtain 3.7 g of the desired product as a colorless oily matter.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05116863
Source datasetuspto-grants-1992_05
ORD IDord-688a02543e90449cb79ab61337b3b473
Source noteuspto-grants-1992_05