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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 402264Generated: October 30, 2026

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

https://huagongshe.com/reaction/402264

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 numberUS08741943B2
Source datasetuspto-grants-2014_06
ORD IDord-95e2f38118db41f58f41fef7ae2489c2
Source noteuspto-grants-2014_06