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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348903Generated: October 25, 2026

N-Methylbutylamine → Methyl 3-{[butyl(methyl)amino]methyl}-5-methylbenzoate

https://huagongshe.com/reaction/348903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylbutylamineHCID 8068—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantMethyl 3-(hydroxymethyl)-5-methylbenzoateHCID 21086184—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-{[butyl(methyl)amino]methyl}-5-methylbenzoateHCID 21086167—

Reaction Conditions

Temperature0 °C

Reaction Steps

To methyl 3-(hydroxymethyl)-5-methylbenzoate prepared by the method in EXAMPLE SP-177 (1.1 g, 6.1 mmol), in anhydrous methylene chloride (10 mL) is added methanesulfonyl chloride (663 μL, 8.6 mmol) at −30° C., and the reaction is warmed to 0° C. The reaction stirred 1 h, then filtered. The filtrate is added to N-methylbutylamine (2.1 mL, 18.3 mmol), and the reaction stirred at room temperature 16 h. The solution is concentrated under reduced pressure. Purification by flash chromatography affords the title compound in pure form. ESI MS m/z 250.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-11bad6c8ad854cd88d2ebe30d073bd0d
Source noteuspto-grants-2007_02