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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylbutylamineHCID 8068—
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethyl 3-bromo-5-(hydroxymethyl)benzoateHCID 11356988—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-bromo-5-{[butyl(methyl)amino]methyl}benzoateHCID 21086161—

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-19cf735d22aa43568555f82b7987d5fd
Source noteuspto-grants-2010_06