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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786627Generated: October 30, 2026

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

https://huagongshe.com/reaction/1786627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminobiphenylHCID 7102—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantMethyl 4-formyl-5-methylfuran-2-carboxylateHCID 15503958—
SolventMethanolHCID 887—
Product4-(Biphenyl-4-ylaminomethyl)-5-methyl-furan-2-carboxylic acid methyl esterHCID 5882419529.1%

Reaction Steps

A solution of biphenyl-4-ylamine (150 mg, 0.883 mmoles) and 4-formyl-5-methyl-furan-2-carboxylic acid methyl ester (157) (135 mg, 0.803 mmoles) in methanol (2.0 ml) was stirred over molecular sieves (type 3 Å) for 1 hour. Sodium cyanoborohydride (55 mg, 0.883 mmoles) was added and the mixture stirred for 18 hour at room temperature. The mixture was concentrated and partitioned between ethyl acetate (25 ml) and saturated aqueous sodium bicarbonate (30 ml). The aqueous phase was re-extracted with ethyl acetate (2×25 ml) and the combined extracts were washed with brine (50 ml) and dried (MgSO4). After removal of the solvent, 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 (75 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07507754B2
Source datasetuspto-grants-2009_03
ORD IDord-42862eee63924cddb9006d6a9ab1e024
Source noteuspto-grants-2009_03