HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14113Generated: October 23, 2026
N-Methylbutylamine → Methyl 3-bromo-5-{[butyl(methyl)amino]methyl}benzoate
https://huagongshe.com/en/reaction/14113
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylbutylamine | HCID 8068 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Methyl 3-bromo-5-(hydroxymethyl)benzoate | HCID 11356988 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Methyl 3-bromo-5-{[butyl(methyl)amino]methyl}benzoate | HCID 21086161 | — |
Reaction Steps
To a solution of methyl 3-bromo-5-(hydroxymethyl)benzoate (4.1 g, 16.8 mmol) in anhydrous methylene chloride (35 mL) at −30° C. is added methanesulfonyl chloride (1.82 mL, 23.5 mmol) followed by triethylamine (4.7 mL, 33.6 mmol). The reaction mixture is stirred for 45 min at 0° C., and then filtered. The filtrate is added to N-methylbutylamine (6 mL, 50.4 mmol) and stirred at room temperature for 16 h. The solution is concentrated under reduced pressure, and the residue is purified by flash column chromatography (silica, 8% ethyl acetate/hexanes) to give the title compound. ESI MS m/z 314.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07727997B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-19cf735d22aa43568555f82b7987d5fd |
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| Source note | uspto-grants-2010_06 |
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