Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 14111Generated: October 26, 2026

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

https://huagongshe.com/reaction/14111

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 numberUS07727997B2
Source datasetuspto-grants-2010_06
ORD IDord-ecb8757435e74c26a364a25fc1369c41
Source noteuspto-grants-2010_06