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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 227865생성일: 2026년 10월 25일

(o-Chlorophenyl)acetonitrile → 2-Biphenylacetonitrile

https://huagongshe.com/reaction/227865

반응식

참여 물질

역할이름HCID투입량
반응물(o-Chlorophenyl)acetonitrileHCID 76112—
반응물Potassium FluorideHCID 522689—
반응물HCID 178419127HCID 178419127—
촉매palladium(II) acetateHCID 167845—
촉매2-(Di-tert-butylphosphino)biphenylHCID 2734215—
용매TetrahydrofuranHCID 8028—
생성물2-BiphenylacetonitrileHCID 33410192.1%

반응 단계

An oven dried resealable Schlenk tube was evacuated and backfilled with argon and charged with palladium acetate (2.2 mg, 0.01 mmol, 1.0 mol %), 2-(di-tert-butylphosphino)biphenyl (6.0 mg, 0.020 mmol, 2.0 mol %), phenylboron dihydroxide (183 mg, 1.5 mmol), and potassium fluoride (174 mg, 3.0 mmol). The tube was evacuated and backfilled with argon, and THF (1 mL) and 2-chlorobenzyl cyanide (152 mg, 1.0 mmol) were added through a rubber septum. The tube was sealed with a teflon screwcap, and the reaction mixture was stirred at room temperature until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (30 mL) and poured into a separatory funnel. The mixture was washed with 1.0 M NaOH (20 mL), and the aqueous layer was extracted with ether (20 mL). The combined organic layers were washed with brine (20 mL), dried over anhydrous magnesium sulfate, filtered, and concentrated. The crude material was purified by flash chromatography on silica gel to afford 178 mg (92%) of the title compound.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07560582B2
출처 데이터셋uspto-grants-2009_07
ORD IDord-0ec155f7e0a7442199f60aea9fd1cde6
출처 메모uspto-grants-2009_07