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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348944Generated: October 29, 2026

Triethylamine → Methyl 3-{[isopentyl(methyl)amino]methyl}-5-methylbenzoate

https://huagongshe.com/reaction/348944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantN,3-Dimethyl-1-butanamineHCID 521020—
ReactantMethyl 3-(hydroxymethyl)-5-methylbenzoateHCID 21086184—
SolventDichloromethaneHCID 6344—
ProductMethyl 3-{[isopentyl(methyl)amino]methyl}-5-methylbenzoateHCID 21086187—

Reaction Steps

To methyl 3-(hydroxymethyl)-5-methylbenzoate prepared by the method in EXAMPLE SP-198, Step 2 in anhydrous methylene chloride at −30° C. is added methanesulfonyl chloride (601 μL, 7.8 mmol), then triethylamine (1.5 mL, 11.1 mmol), and the reaction is stirred at 0° C. 15 min. The resulting precipitate is filtered, and the filtrate is added to N-methylisoamylamine (2.1 mL, 16.7 mmol). The reaction stirred at room temperature 16 h. The solution is concentrated under reduced pressure, redissolved in ethyl acetate and washed with saturated sodium bicarbonate, brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 20% ethyl acetate/hexanes) provides the title compound. ESI MS m/z 264.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176242B2
Source datasetuspto-grants-2007_02
ORD IDord-b8e6fb4a9c3d41e9be0fa9a622b67128
Source noteuspto-grants-2007_02