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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243908Generated: October 26, 2026

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

https://huagongshe.com/reaction/1243908

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 (116 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 retained. The aqueous layer was extracted with toluene and combined with the organic layer obtained earlier, and 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07119215B2
Source datasetuspto-grants-2006_10
ORD IDord-07e141aed5554b55beab04c8b533906b
Source noteuspto-grants-2006_10