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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823118Generated: November 3, 2026

Benzaldehyde → Methyl 4'-[2-(benzylamino)ethyl]-1,1'-biphenyl-4-carboxylate

https://huagongshe.com/reaction/1823118

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzaldehydeHCID 240—
ReactantMethyl 4'-(2-aminoethyl)-1,1'-biphenyl-4-carboxylate hydrochlorideHCID 22171302—
SolventDichloromethaneHCID 6344—
ProductMethyl 4'-[2-(benzylamino)ethyl]-1,1'-biphenyl-4-carboxylateHCID 2217157392.5%

Reaction Steps

To a solution of methyl 4′-(2-aminoethyl)-1,1′-biphenyl-4-carboxylate hydrochloride (420 mg) and benzaldehyde (153 mg) in dichloromethane (5 ml) was stirred for 3 hours, and the mixture was evaporated in vacuo. To the residue in methanol (10 ml) was added sodium borohydride (65 mg) on ice cooling, and stirred at the same temperature for 1 hour. The resulting mixture was poured into saturated aqueous sodium bicarbonate solution, and extracted with ethyl acetate. The organic layer was washed with brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was chromatographed (hexane—ethyl acetate) over silica gel to afford methyl 4′-[2-(benzylamino)ethyl]-1,1′-biphenyl-4-carboxylate (460 mg) as a colorless powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07037938B2
Source datasetuspto-grants-2006_05
ORD IDord-5324d17a414b43ea86ce8983b2f7d27c
Source noteuspto-grants-2006_05