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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766036Generated: November 1, 2026

Methyl iodide → 2-Chloro-3-methoxybenzaldehyde

https://huagongshe.com/reaction/1766036

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-3-hydroxybenzaldehydeHCID 593376—
SolventDimethylformamideHCID 6228—
Product2-Chloro-3-methoxybenzaldehydeHCID 12575695—

Reaction Steps

To a solution of 2-chloro-3-hydroxybenzaldehyde (4.55 g, 29 mmol) in DMF (30 mL) was added K2CO3 (4.8 g, 34.9 mmol) followed by MeI (2.7 mL, 43.6 mmol), and the mixture was stirred at room temperature for 16 hours. Following concentration in vacuo, the residual was taken up in ethyl acetate, washed with H2O, brine, dried over Na2SO4, and concentrated. Purification by column chromatography on silica gel with ethyl acetate/hexanes 1/5 afforded 2-chloro-3-methoxybenzaldehyde 3a (4.68 g, 94%) as a colorless oil, which solidified upon standing. GCMS (EI) m/z 170, 172 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07229995B2
Source datasetuspto-grants-2007_06
ORD IDord-556a1851494844d5b067e45b09f767e3
Source noteuspto-grants-2007_06