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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928938Generated: November 1, 2026

Water → Methyl 5-((4-bromo-2-formylphenyl)(4-methoxybenzyl)amino)pentanoate

https://huagongshe.com/reaction/1928938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-((4-Bromo-2-formylphenyl)(4-methoxybenzyl)amino)pentanoic acidHCID 11495447—
SolventDimethylformamideHCID 6228—
ProductMethyl 5-((4-bromo-2-formylphenyl)(4-methoxybenzyl)amino)pentanoateHCID 1157566957.3%

Reaction Steps

To a solution of 5-((4-bromo-2-formylphenyl)(4-methoxybenzyl)amino)pentanoic acid (77.2 g) and potassium carbonate (30.5 g) in DMF (500 ml) was added dropwise a solution of iodomethane (36.5 g) in DMF (100 ml) at 0° C. under nitrogen atmosphere. After stirring for 2 hours, water was added and the mixture was extracted with ethyl acetate. After washing the organic layer with water three times and with saturated brine once, the resultant was dried with magnesium sulfate. The solvent was distilled off under reduced pressure and the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1→hexane:ethyl acetate=4:1) to give methyl 5-((4-bromo-2-formylphenyl)(4-methoxybenzyl)amino)-pentanoate (45.7 g) as a brown oily material.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183273B2
Source datasetuspto-grants-2012_05
ORD IDord-d28b8ec295cd482aa0ef6e0b206c8aeb
Source noteuspto-grants-2012_05