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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258337Generated: October 30, 2026

Methyl iodide → 3-Chloro-4-methoxybenzaldehyde

https://huagongshe.com/reaction/1258337

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 numberUS08466148B2
Source datasetuspto-grants-2013_06
ORD IDord-03c69c58f38946979c9eee88d11d220f
Source noteuspto-grants-2013_06