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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1375002Generated: October 30, 2026

Iodine → 4-Fluoro-3-methylbenzaldehyde

https://huagongshe.com/reaction/1375002

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantSulfuric AcidHCID 1118—
Reactant5-Bromo-2-fluorotolueneHCID 123527—
ReactantMagnesiumHCID 5462224—
ReactantEthylorthoformateHCID 53630039—
SolventDiethyl EtherHCID 3283—
Product4-Fluoro-3-methylbenzaldehydeHCID 2734874—

Reaction Steps

A solution of 5-bromo-2-fluorotoluene (6 g) in ethyl ether (10 ml) and a catalytic amount of iodine were added to a suspension of magnesium (960 mg) in ethyl ether (10 ml) under nitrogen atmosphere and the whole was refluxed for 30 minutes. After cooling, a solution of ethyl orthoformate (5.4 g) in ethyl ether (20 ml) was added to the mixture and the whole was stirred overnight. Sulfuric acid (10%, 20 ml) was added to the mixture and the organic layer was separated, washed with brine, dried over sodium sulfate, and evaporated. The residue was purified by column chromatography on silica gel with a mixture of hexane and ethyl acetate (10:1) as eluent to give 4-fluoro-3-methylbenzaldehyde as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07166598B2
Source datasetuspto-grants-2007_01
ORD IDord-98632e66786e46c59a1afab21c3c510e
Source noteuspto-grants-2007_01