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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041807Generated: November 1, 2026

Sodium Carbonate → 4-Propyl-1-(3-chloro-5-fluorophenyl)benzene

https://huagongshe.com/reaction/2041807

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant1-Bromo-3-chloro-5-fluorobenzeneHCID 2736223—
Reactant(4-Propylphenoxy)boronic acidHCID 21869456—
ReactantEthanol toluene waterHCID 86587398—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product4-Propyl-1-(3-chloro-5-fluorophenyl)benzeneHCID 5930398097.7%

Reaction Steps

At first, 25.8 g of 4-propylphenylboric acid (S1-1), 30.0 g of 1-bromo-3-chloro-5-fluorobenzene (S1-2), 2.5 g of tetrakis(triphenylphosphine)palladium, 50.1 g of sodium carbonate and 700 ml of a mixed solvent of toluene/ethanol/water=3/3/1 (volume ratio) were added into a reactor under nitrogen atmosphere, and then the mixture was refluxed for 5 hours. Next, the reaction solution was cooled to room temperature, added with toluene and then washed with 1N hydrochloric acid and water. Then, the resulting solution was dried over magnesium sulfate and then distilled under reduced pressure to remove the solvent. The residue was purified by silica-gel column chromatography with heptane as eluent and then dried under reduced pressure to obtain 34.8 g of 4-propyl-1-(3-chloro-5-fluorophenyl)benzene (S1-3). The yield of the compound (S1-3) from (S1-1) was 97.7%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08586153B2
Source datasetuspto-grants-2013_11
ORD IDord-a9d848b43920476197e11fd537bfb1fe
Source noteuspto-grants-2013_11