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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1776361Generated: November 1, 2026

Methyl iodide → 3-Chloro-4-methoxybenzaldehyde

https://huagongshe.com/reaction/1776361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-4-hydroxybenzaldehydeHCID 17022—
SolventDimethylformamideHCID 6228—
Product3-Chloro-4-methoxybenzaldehydeHCID 7861993%

Reaction Steps

To a stirred solution of 3-chloro-4-hydroxybenzaldehyde (2.9 g, 18.412 mmol) in DMF (30 mL) was added K2CO3 (7.6 g, 55.238 mmol). CH3I (7.80 g, 55.238 mmol) was then added slowly at RT under an inert atmosphere. After addition was completed, the reaction mixture was brought to 80° C. and stirred for 1 h. The reaction mixture was quenched with water (20 mL) and extracted with EtOAc (2×50 mL). The combined organic layers were washed with water and brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo to obtain crude product. The crude material was purified via silica gel column chromatography to afford 3-chloro-4-methoxybenzaldehyde (2.78 g, 93%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09265767B2
Source datasetuspto-grants-2016_02
ORD IDord-5ff29f9a5586431b9e7dd0c38b0a8be3
Source noteuspto-grants-2016_02