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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1750797Generated: October 30, 2026

Potassium Carbonate → 2-Chloro-1-fluoro-4-(3,3,3-trifluoroprop-1-en-2-yl)benzene

https://huagongshe.com/reaction/1750797

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Propene, 2-bromo-3,3,3-trifluoro-HCID 272696—
Reactant3-Chloro-4-fluorophenylboronic Acid (contains varying amounts of Anhydride)HCID 2734660—
CatalystHCID 178418476HCID 178418476—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Chloro-1-fluoro-4-(3,3,3-trifluoroprop-1-en-2-yl)benzeneHCID 6682388562.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of (3-chloro-4-fluorophenyl)boronic acid (300 mg, 1.72 mmol), 2-bromo-3,3,3-trifluoroprop-1-ene (331 mg, 1.89 mmol), K2CO3 (474 mg, 3.44 mmol) and Pd(PPh3)2Cl2 (25 mg, 0.035 mmol) in THF (2 mL) and H2O (1 mL) was heated at 80° C. in a sealed tube for 3 h. The mixture was cooled to rt and partitioned between EA (20 mL) and H2O (20 mL). The aqueous layer was extracted with EA (20 mL) and the combined organic layers were dried over Na2SO4. The solvent was removed under reduced pressure and the crude product was purified by column chromatography on silica gel elute with PE to give 2-chloro-1-fluoro-4-(3,3,3-trifluoroprop-1-en-2-yl)benzene (240 mg, 62.3% yield) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09156860B2
Source datasetuspto-grants-2015_10
ORD IDord-1fee94b06d9746658b63511037276c13
Source noteuspto-grants-2015_10