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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611054Generated: November 1, 2026

Methyl Salicylate → Methyl 2-(1-methoxycarbonylpentoxy)benzoate

https://huagongshe.com/reaction/1611054

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl SalicylateHCID 4133—
ReactantPotassium CarbonateHCID 11430—
ReactantHexanoic acid, 2-bromo-, methyl esterHCID 95578—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-(1-methoxycarbonylpentoxy)benzoateHCID 10446375—

Reaction Steps

15.2 g of methyl salicylate and 18.0 g of potassium carbonate were introduced into 125 ml of acetonitrile in a 250 ml flask under an argon atmosphere and, at room temperature, 20.9 g of methyl 2-bromohexanoate were added. The colourless suspension was heated under reflux with stirring for 16 hours, and the progress of the reaction was checked by thin-layer chromatography. After cooling to room temperature, the suspension was filtered and the residue was washed with acetone. Concentration of the filtrate in vacuo resulted in 27.8 g (99% of theory) of methyl 2-(1-methoxycarbonylpentoxy)benzoate as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06984741B2
Source datasetuspto-grants-2006_01
ORD IDord-414dc2d4881d4e1091e5276df4aa6c33
Source noteuspto-grants-2006_01