Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1243910Generated: October 31, 2026

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

https://huagongshe.com/reaction/1243910

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Bromo-4-fluorobenzeneHCID 9993—
ReactantAmmonium ChlorideHCID 25517—
Reactant2,4-DimethylbenzaldehydeHCID 61814—
ReactantMagnesiumHCID 5462224—
CatalystIodineHCID 807—
Catalyst1-Bromo-4-fluorobenzeneHCID 9993—
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 (46 ml), and iodine (0.1 g) was added. Then, 4-bromofluorobenzene (2.1 g) was added dropwise. After confirmation of the start of the reaction, THF (242 ml) was flown in. 4-Bromofluorobenzene (113.9 g) was added dropwise at 31.8–48.9° C., and the mixture was stirred at 38–40° C. for 2 hr. The obtained mixture with a Grignard reagent was cooled and thereto was added dropwise 2,4-dimethylbenzaldehyde (81 g) at 5–29.9° C. After the dropwise addition, the reaction mixture was stirred at 21.3–28.3° C. for 1.5 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-28a4b1d8111846b79a81d3766285b134
Source noteuspto-grants-2006_10