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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243909Generated: October 30, 2026

1-Bromo-4-fluorobenzene → (2,4-Dimethylphenyl)(4-fluorophenyl)methanol

https://huagongshe.com/reaction/1243909

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantAmmonium ChlorideHCID 25517—
Reactant2,4-DimethylbenzaldehydeHCID 61814—
ReactantMagnesiumHCID 5462224—
CatalystIodineHCID 807—
SolventTetrahydrofuranHCID 8028—
Product(2,4-Dimethylphenyl)(4-fluorophenyl)methanolHCID 9899421100.1%

Reaction Steps

Under a nitrogen atmosphere, turnings of magnesium (16.8 g) were dispersed in THF (54 ml), and iodine (0.1 g) was added. Under a nitrogen atmosphere, a solution of 4-bromofluorobenzene (116 g) in THF (201 ml) was added dropwise at 15–40° C., and the mixture was stirred at 20–40° C. for 2 hr. The obtained mixture with a Grignard reagent was cooled and thereto was added dropwise a solution of 2,4-dimethylbenzaldehyde (81 g) in THF (81 ml) at 0–20° C. After the dropwise addition, the reaction mixture was stirred at 0–20° C. for 2 hr. A saturated aqueous ammonium chloride solution was added to stop the reaction. The reaction mixture was partitioned and the obtained organic layer was washed with saturated brine. The solvent was evaporated from the organic layer under reduced pressure to give (2,4-dimethylphenyl)-(4′-fluorophenyl)methanol (139.2 g, 100%) as a colorless oil. The obtained colorless oil was measured for 1H-NMR and found to be the same as in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119215B2
Source datasetuspto-grants-2006_10
ORD IDord-914607226800452f9515b68e2bae568f
Source noteuspto-grants-2006_10