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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458390Generated: November 3, 2026

Potassium Carbonate → 4-(p-Chlorophenyl)-3-fluoro-1-(4-fluoro-3-phenoxyphenyl)-4-methyl-2-pentene

https://huagongshe.com/reaction/1458390

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(4-Fluoro-3-phenoxyphenyl)-boronic acidHCID 21185404—
ReactantMethylenechloride HexaneHCID 21226440—
Reactant1-Bromo-4-(p-chlorophenyl)-3-fluoro-4-methyl-2-penteneHCID 54272913—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
Product4-(p-Chlorophenyl)-3-fluoro-1-(4-fluoro-3-phenoxyphenyl)-4-methyl-2-penteneHCID 5454256885.6%

Reaction Steps

A mixture of 1-bromo-4-(p-chlorophenyl)-3-fluoro-4-methyl-2-pentene, (Z)- (1.02 g, 3.5 mmol), and bis(di-benzylideneacetone)palladium(0) (Pd(dba)2, 0.1 g, 0.17 mmol) in toluene (20 mL) under nitrogen is stirred for one minute, treated with potassium carbonate (1.94 g, 0.014 mol), degassed, treated with a solution of 4-fluoro-3-phenoxybenzeneboronic acid (1.05 g, 4.55 mmol) in ethanol (5 mL), refluxed for 50 minutes, cooled to room temperature, diluted with ethyl acetate and filtered through diatomaceous earth. The filtrate is washed sequentially with water and brine, dried over anhydrous sodium sulfate and concentrated in vacuo to obtain a residue. Flash chromatography of the residue using silica gel and a 15:100 methylene chloride/hexane solution gives the title compound as a colorless oil (1.19 g, 85.6% yield) which is identified by NMR spectral analyses.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05849958
Source datasetuspto-grants-1998_12
ORD IDord-deeaaa57cec5403a808655c6a2742276
Source noteuspto-grants-1998_12