戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1296977作成日:2026年10月26日

4-Chlorotoluene → 4-Hexylanisole

https://huagongshe.com/reaction/1296977

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorotolueneHCID 7810—
反応物1,4-DioxaneHCID 31275—
反応物Boronic AcidHCID 61668—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物2,6-Dimethyl-N-(n-hexyl)anilineHCID 10987409—
触媒palladium(II) acetateHCID 167845—
生成物4-HexylanisoleHCID 578599—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07247731B2
出典データセットuspto-grants-2007_07
ORD IDord-a382e65e648b4e1abb7ae64fad4aa7df
出典メモuspto-grants-2007_07