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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968971Generated: October 29, 2026

3-Chloro-2-methyl-1-propene → 1-Chloro-2-fluoro-4-(2-methylprop-2-en-1-yl)benzene

https://huagongshe.com/reaction/968971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chloro-2-methyl-1-propeneHCID 11241—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantAmmonium ChlorideHCID 25517—
Reactant4-Bromo-1-chloro-2-fluorobenzeneHCID 2724690—
ReactantMagnesiumHCID 5462224—
CatalystIodineHCID 807—
CatalystCopper iodideHCID 83717—
SolventTetrahydrofuranHCID 8028—
Product1-Chloro-2-fluoro-4-(2-methylprop-2-en-1-yl)benzeneHCID 23109556—

Reaction Steps

Magnesium (2.43 g) and iodine (10 mg) were added to tetrahydrofuran (40 ml) and a solution of 4-bromo-1-chloro-2-fluorobenzene (21.0 g) in tetrahydrofuran (40 ml) was added dropwise, and the mixture was stirred at room temperature for 1 hr to give a Grignard's reagent. The reaction mixture was ice-cooled and copper iodide (1.90 g) was added. 3-Chloro-2-methyl-1-propene (14.8 ml) was added and the mixture was stirred at room temperature for 1 hr. The reaction mixture was ice-cooled and saturated aqueous ammonium chloride solution (10 ml) was added. The mixture was stirred at room temperature for 20 min and magnesium sulfate (40 g) was added. The reaction mixture was filtered and the filtrate was concentrated under reduced pressure. Hexane (100 ml) was added to the obtained residue and insoluble materials were filtered off. The resulting solution was concentrated under reduced pressure to give the title compound (16.9 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07304174B2
Source datasetuspto-grants-2007_12
ORD IDord-2c244ac55eec4504814a6f9824bcfb52
Source noteuspto-grants-2007_12