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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-((4-Bromo-2-formylphenyl)(isobutyl)amino)pentanoic acid | HCID 86595582 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | methyl 5-(4-bromo-2-formyl-N-isobutylanilino)pentanoate | HCID 86595583 | 84% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08741943B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-95e2f38118db41f58f41fef7ae2489c2 |
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| Source note | uspto-grants-2014_06 |
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