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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1106797Generated: October 31, 2026

Methyl 4-aminobenzoate → Methyl 4-[N-(5-bromo-2-(phenethyl)benzyl)amino]benzoate

https://huagongshe.com/reaction/1106797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-aminobenzoateHCID 12082—
Reactant5-Bromo-2-(phenethyl)benzaldehydeHCID 22675482—
SolventTolueneHCID 1140—
ProductMethyl 4-[N-(5-bromo-2-(phenethyl)benzyl)amino]benzoateHCID 2267557089.1%

Reaction Steps

5-Bromo-2-(phenethyl)benzaldehyde (1.27 g) and methyl 4-aminobenzoate (0.66 g) were heated together at 110° C. for 30 minutes and for a further 30 minutes under vacuum. The mixture was dissolved in toluene, evaporated to dryness, dissolved in ethanol (15 ml). Sodium borohydride (0.33 g) was added, the mixture stirred for 18 hours, the solvent evaporated and the residue mixed with acetic acid and partitioned between saturated aqueous sodium hydrogen carbonate and ethyl acetate. The organic layer was washed with brine, dried (MgSO4), filtered and evaporated. The resulting residue was purified by MPLC, eluting with dichloromethane, to give methyl 4-[N-(5-bromo-2-(phenethyl)benzyl)amino]benzoate (1.65 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057345
Source datasetuspto-grants-2000_05
ORD IDord-3b07cf6361084adabf869036d3cb30f6
Source noteuspto-grants-2000_05