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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 355779Generated: October 28, 2026

Water → tert-Butyl 4-[N-(5-bromo-2-benzyloxybenzyl)-N-(4-methoxycarbonylbenzyl)amino]benzoate

https://huagongshe.com/reaction/355779

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 4-(bromomethyl)benzoateHCID 256687—
Reactanttert-Butyl 4-[5-bromo-2-benzyloxybenzylamino]benzoateHCID 22675479—
SolventDimethylformamideHCID 6228—
Producttert-Butyl 4-[N-(5-bromo-2-benzyloxybenzyl)-N-(4-methoxycarbonylbenzyl)amino]benzoateHCID 22675539—

Reaction Steps

tert-Butyl 4-[5-bromo-2-benzyloxybenzylamino]benzoate (16.9 g) and methyl-4-bromomethylbenzoate were dissolved in in dimethylformamide (30 ml) and potassium carbonate (18 g) added. The mixture was stirred at ambient temperature for 24 hours and then poured into water (300 ml). The reaction mixture was extracted with ether (4×100 ml). The combined ether extracts were washed with water (3×100 ml) and brine (1×100 ml), dried over magnesium sulphate and evaporated. The residue was purified by MPLC eluting with 1:1 dichloromethane/hexane to give tert-butyl 4-[N-(5-bromo-2-benzyloxybenzyl)-N-(4-methoxycarbonylbenzyl)amino]benzoate (3.6 g) m.p. 154°-155° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05834468
Source datasetuspto-grants-1998_11
ORD IDord-39f8e0da2b33463c87c209eb1f1e8751
Source noteuspto-grants-1998_11