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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1768932생성일: 2026년 10월 26일

4-Bromoanisole → 2-(4-Methoxyphenyl)benzonitrile

https://huagongshe.com/reaction/1768932

반응식

참여 물질

역할이름HCID투입량
반응물4-BromoanisoleHCID 7730—
반응물2-BromobenzonitrileHCID 16272—
반응물ButyllithiumHCID 178418339—
촉매ZincchlorideHCID 3007855—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매Diethyl EtherHCID 3283—
용매TetrahydrofuranHCID 8028—
용매HexaneHCID 8058—
생성물2-(4-Methoxyphenyl)benzonitrileHCID 1393373—

반응 단계

To a solution of 4-bromoanisole (18.7 g, 0.1 mol) in anhydrous tetrahydrofuran (200 mL) at -78° C. was added a solution of n-butyl lithium (2.5M, 50 mL) in hexane. After stirring for 0.5 hours, a solution of the zinc chloride (1M, 100 mL) in ether was added. After the mixture was stirred for 1 hour at -78° C., tetrakis (triphenylphosphine) palladium (0.85 g, 0.73 mmol) and 2-bromobenzonitrile (18.2 g, 0.1 mol) were added. The reaction mixture was stirred at room temperature overnight, and then was concentrated in vacuo. The residue was partitioned between ethyl acetate (100 mL) and 1N hydrochloric acid (100 mL). The organic solution was washed with brine and dried over magnesium sulfate. Concentration in vacuo gave crude 4-(2-cyanophenyl)anisole, which was directly used for next reaction. The compound can be triturated with ether to obtain a pure solid product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05380719
출처 데이터셋uspto-grants-1995_01
ORD IDord-7842e73193204e33a44698038c9ab303
출처 메모uspto-grants-1995_01