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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874470Generated: October 30, 2026

Hydrochloric Acid → N-{[3-(Benzyloxy)phenyl]methyl}-2-([1,1'-biphenyl]-4-yl)acetamide

https://huagongshe.com/reaction/874470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFelbinacHCID 3332—
ReactantDiisopropylethylamineHCID 81531—
ReactantPyBOPHCID 2724699—
Reactant[3-(Benzyloxy)phenyl]methanamine hydrochlorideHCID 19744718—
ReactantHCID 178506432HCID 178506432—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-{[3-(Benzyloxy)phenyl]methyl}-2-([1,1'-biphenyl]-4-yl)acetamideHCID 5900062162.2%

Reaction Steps

To a solution of 4-biphenyl acetic acid (2.29 g, 10.45 mmol) in dimethylformamide, DMF, (30 ml) was added diisopropylethylamine, DIEA, (5.47 ml, 31.35 mmol) and stirred at room temperature for 15 min, then benzotriazolyloxy-tris[pyrrolidino]-phosphonium hexafluorophosphate, PyBOP™, (5.43 g, 10.45 mmol) was added and the stirring was continued for further 30 min, then 3-benzyloxybenzylaminehydrochloride (2.6 g, 10.45 mmol) was added and the stirring continued for 24 hrs. The reaction mixture was then poured on to ice cooled water acidified with (10 ml) 1 N HCl and extracted with ethyl acetate (100 ml) and the organic layer washed with saturated solution of NaHCO3, water and brine, dried over Na2SO4 and the solvent removed under vacuum to give a yellowish-white powder of the desired compound (2.65 g) 62% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980890B2
Source datasetuspto-grants-2015_03
ORD IDord-4e2a4fea897b4b2894a8a3cbe705018a
Source noteuspto-grants-2015_03