Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266854Generated: November 2, 2026

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

https://huagongshe.com/reaction/2266854

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

D 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 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 numberUS07858644B2
Source datasetuspto-grants-2010_12
ORD IDord-d514bb5dfb1b4057ab65cfb9d0a1a0ab
Source noteuspto-grants-2010_12