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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 53997Generated: October 26, 2026

Methyl 4-Formylbenzoate → Methyl 4-[2-(5-cyano-2-benzofuranyl)vinyl]benzoate

https://huagongshe.com/reaction/53997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-FormylbenzoateHCID 15294—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(5-Cyano-2-benzofuranyl)methyltriphenylphosphonium chlorideHCID 21844326—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4-[2-(5-cyano-2-benzofuranyl)vinyl]benzoateHCID 54344271—

Reaction Steps

5.17 g of methyl 4-formylbenzoate and 13.97 g of (5-cyano-2-benzofuranyl)methyltriphenylphosphonium chloride were dissolved in a solvent mixture of 50 ml of tetrahydrofuran and 50 ml of methanol. A 5.02 g of 1,8-diazabicyclo[5.4.0]-7-undecene was added to the thus prepared solution while stirring under ice cooling, followed by stirring at room temperature for 2 hours. By collecting the precipitated crystals through a filter, methyl 4-[2-(5-cyano-2-benzofuranyl)vinyl]benzoate was obtained as a mixture of E and Z forms. The thus obtained crystals were dissolved in a solvent mixture of 300 ml of tetrahydrofuran and 100 ml of ethanol, and the solution was subjected to catalytic hydrogenation under normal pressure for 2 hours in the presence of 2.0 g of palladium oxide.1H2O.barium sulfate. After removing the catalyst by filtration and concentrating the resulting filtrate, the thus obtained residue was purified by subjecting it to silica gel column chromatography using benzene as an elution solvent to obtain 8.1 g of methyl 4-[2-(5-cyano-2-benzofuranyl)ethyl]benzoate in the form of prism crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05620991
Source datasetuspto-grants-1997_04
ORD IDord-ce510db4f3744e21867e88c4dcf8e68a
Source noteuspto-grants-1997_04