Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1928933Generated: November 1, 2026

Water → methyl 5-(4-bromo-2-formyl-N-isobutylanilino)pentanoate

https://huagongshe.com/reaction/1928933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant5-((4-Bromo-2-formylphenyl)(isobutyl)amino)pentanoic acidHCID 86595582—
SolventDimethylformamideHCID 6228—
Productmethyl 5-(4-bromo-2-formyl-N-isobutylanilino)pentanoateHCID 8659558384%

Reaction Steps

To a suspension of 5-(4-bromo-2-formyl-N-isobutylanilino)pentanoic acid (15.0 g), potassium carbonate (7.0 g) in DMF (50 ml) was added dropwise a solution of iodomethane (8.4 g) in DMF (10 ml) at 0° C. under a nitrogen atmosphere. The mixture was warmed to room temperature, and stirred for 2 hours under a nitrogen atmosphere. After addition of water, the solution was extracted with ethyl acetate. The organic layer was washed with water and saturated saline, and dried over magnesium sulfate. After distilling off the solvent under reduced pressure, the resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=9:1 to hexane:ethyl acetate=1:1) to obtain brown oil of methyl 5-(4-bromo-2-formyl-N-isobutylanilino)pentanoate (13.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08183273B2
Source datasetuspto-grants-2012_05
ORD IDord-3a39cafd62e64757861aadd07c50daf6
Source noteuspto-grants-2012_05