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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277145Generated: October 25, 2026

Methyl iodide → 3-Benzyloxy-6-methoxypicolinic acid

https://huagongshe.com/reaction/277145

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantAcetone hexaneHCID 21880519—
ReactantMethyl 3-benzyloxy-6-methoxypicolinateHCID 22175139—
CatalystHCID 178418647HCID 178418647—
SolventTolueneHCID 1140—
Product3-Benzyloxy-6-methoxypicolinic acidHCID 17817634—

Reaction Conditions

Temperature60 °C

Reaction Steps

To a stirred solution of this compound (10.25 g) in toluene (125 mL), warmed in an oil bath at 60° C. was added silver carbonate (16.6 g), then methyl iodide (8.52 g). The resulting mixture was stirred and heated for 3 hours at 60° C. After cooling, the mixture was filtered through Celite® and the solvent evaporated to give a yellow oil. Silica gel chromatography (4:1 hexane/acetone) gave a nearly colorless oil, whose 1H-NMR and MS data were consistent with methyl 3-benzyloxy-6-methoxypicolinate. Hydrolysis of this ester to the title acid 18 was accomplished with LiOH.H2O as described above for related esters.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355660B1
Source datasetuspto-grants-2002_03
ORD IDord-e11e2406b5c345c5a328d12f46afef2b
Source noteuspto-grants-2002_03