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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460102Generated: October 29, 2026

Potassium Iodide → 4-(Biphenyl-4-ylaminomethyl)-5-methyl-furan-2-carboxylic acid methyl ester

https://huagongshe.com/reaction/460102

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
Reactant4-AminobiphenylHCID 7102—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-(chloromethyl)-5-methylfuran-2-carboxylateHCID 914782—
SolventTetrahydrofuranHCID 8028—
Product4-(Biphenyl-4-ylaminomethyl)-5-methyl-furan-2-carboxylic acid methyl esterHCID 5882419571.1%

Reaction Steps

Potassium iodide (32 mg) and a solution of biphenyl-4-ylamine (74 mg, 0.438 mmoles) in tetrahydrofuran (1 ml) was added to a mixture of 4-chloromethyl-5-methyl-furan-2-carboxylic acid methyl ester (159)(75 mg, 0.398 mmoles) and potassium carbonate (83 mg) in tetrahydrofuran (1 ml). The mixture was stirred at room temperature under an argon atmosphere for 16 hours, and then refluxed with the exclusion of light for 16 hours. After cooling, the mixture was concentrated and the residue was purified by by flash chromatography, using a gradient elution of petrol/diethyl ether 9:1 v/v to 4:1 v/v, to afford compound 158(91 mg). LC/MS System A; Rt=3.93 mins, m/z (ES+)=322(M+H for C20H19NO3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196089B2
Source datasetuspto-grants-2007_03
ORD IDord-60e6b15a06644dc7ad77916cb1b2572a
Source noteuspto-grants-2007_03