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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1006004Generated: October 30, 2026

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

https://huagongshe.com/reaction/1006004

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 numberUS06787562B2
Source datasetuspto-grants-2004_09
ORD IDord-f4237f4814b44882a9fe6d7bdf572365
Source noteuspto-grants-2004_09