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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 460103Generated: October 29, 2026

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

https://huagongshe.com/reaction/460103

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Biphenyl-4-ylaminomethyl)-5-methyl-furan-2-carboxylic acid methyl esterHCID 58824195—
SolventTetrahydrofuranHCID 8028—
Product4-(Biphenyl-4-ylaminomethyl)-5-methyl-furan-2-carboxylic acidHCID 1844458440.2%

Reaction Steps

A solution of 4-(biphenyl-4-ylaminomethyl)-5-methyl-furan-2-carboxylic acid methyl ester (158) (91 mg, 0.283 mmoles) in dry tetrahydrofuran (5 ml) was treated with potassium trimethylsilanoate (182 mg, 1.42 mmoles) and the mixture stirred under an argon atmosphere for 3 hours. After evaporation of the solvent, the residue was purified by HPLC (gradient: 15% acetonitrile/85% water containing 0.1% trifluoroacetic acid to 55% acetonitrile/45% water at a rate of 1%/min) to afford compound 160(35 mg) as a white solid. LC/MS System D; Rt=7.64 mins, m/z (ES+)=308 (M+H for C19H17NO3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07196089B2
Source datasetuspto-grants-2007_03
ORD IDord-cddf2e14808945e2bf789f497ceee6dd
Source noteuspto-grants-2007_03