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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365585Generated: October 29, 2026

Methyl Salicylate → N-Butylsalicylamide

https://huagongshe.com/reaction/1365585

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl SalicylateHCID 4133—
ReactantButylamineHCID 8007—
SolventMethanolHCID 887—
ProductN-ButylsalicylamideHCID 9361879%

Reaction Steps

10.0 g (65.7 mmol) of methyl salicylate and 33 ml of n-butylamine were dissolved in 100 ml of methanol, followed by heating at reflux for 8 hours while stirring. Methanol was distilled off under reduced pressure, and the residue was acidified by adding an aqueous 2 N hydrochloric acid, followed by extraction with dichloromethane. The organic layer was washed in turn with water and saturated sodium hydrogen carbonate, and then dried over anhydrous magnesium sulfate. The organic layer was filtered, and the filtrate was concentrated under reduced pressure, and then the resulting residue was purified by silica gel column chromatography (eluant hexane/ethyl acetate=10/1 to 5/1) to obtain 10.0 g (yield: 79%) of salicylic acid n-butylamide as an oily substance. 1H—NMR spectrum data of salicylic acid n-butylamide are as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07892711B2
Source datasetuspto-grants-2011_02
ORD IDord-edce66150fc141d598382b73f36e27ed
Source noteuspto-grants-2011_02