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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227843Generated: October 25, 2026

4-Chlorotoluene → 4-Hexylanisole

https://huagongshe.com/reaction/227843

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-ChlorotolueneHCID 7810—
Reactant1,4-DioxaneHCID 31275—
ReactantBoronic AcidHCID 61668—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant2,6-Dimethyl-N-(n-hexyl)anilineHCID 10987409—
Catalystpalladium(II) acetateHCID 167845—
Product4-HexylanisoleHCID 578599—

Reaction Steps

General procedure for K3PO4 promoted Suzuki coupling of aryl chlorides: An oven-dried resealable Schlenk tube was purged with argon and charged with Pd(OAc)2 (0.01 mmol, 0.5 mol %), ligand 2 (0.015 mmol, 0.75 mol %), the boronic acid (3.0 mmol), and potassium phosphate (4.0 mmol). The tube was purged with argon, and dioxane (6 mL) and 4-chlorotoluene (2.0 mmol) were added through a rubber septum. The septum was removed, the tube was sealed with a teflon screw cap and the mixture was stirred at room temperature for 2 min, then heated to 100° C. with stirring until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was then cooled to room temperature, diluted with ether (20 mL) and poured into a separatory funnel. The mixture was washed with 1 M NaOH (20 mL), and the layers were separated. The aqueous layer was extracted with ether (20 mL), and the combined organic layers were dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude material was then purified by flash chromatography on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560582B2
Source datasetuspto-grants-2009_07
ORD IDord-0d117de3c0034e8485d180e97dbf4205
Source noteuspto-grants-2009_07