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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1810778Generated: October 31, 2026

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

https://huagongshe.com/reaction/1810778

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 numberUS08362058B2
Source datasetuspto-grants-2013_01
ORD IDord-59f59cfae2d54007a2b37dd716cf7280
Source noteuspto-grants-2013_01