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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1296977생성일: 2026년 10월 24일

4-Chlorotoluene → 4-Hexylanisole

https://huagongshe.com/ko/reaction/1296977

반응식

참여 물질

역할이름HCID투입량
반응물4-ChlorotolueneHCID 7810—
반응물1,4-DioxaneHCID 31275—
반응물Boronic AcidHCID 61668—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물2,6-Dimethyl-N-(n-hexyl)anilineHCID 10987409—
촉매palladium(II) acetateHCID 167845—
생성물4-HexylanisoleHCID 578599—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07247731B2
출처 데이터셋uspto-grants-2007_07
ORD IDord-a382e65e648b4e1abb7ae64fad4aa7df
출처 메모uspto-grants-2007_07