HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222828Generated: October 31, 2026
Water → Methyl 5-((4-bromo-2-formylphenyl)(4-methoxybenzyl)amino)pentanoate
https://huagongshe.com/reaction/2222828
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)(4-methoxybenzyl)amino)pentanoic acid | HCID 11495447 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Methyl 5-((4-bromo-2-formylphenyl)(4-methoxybenzyl)amino)pentanoate | HCID 11575669 | 57.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371772B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-43e7f390b7af465997656ce085a1cc9f |
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| Source note | uspto-grants-2008_05 |
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