돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 76097생성일: 2026년 10월 24일

6-Bromo-3,5-dimethoxypicolinonitrile → 6-Ethyl-3,5-dimethoxy-pyridine-2-carbonitrile

https://huagongshe.com/ko/reaction/76097

반응식

참여 물질

역할이름HCID투입량
반응물6-Bromo-3,5-dimethoxypicolinonitrileHCID 73554911—
반응물HCID 178418443HCID 178418443—
촉매Dichloro(1,1'-(1,3-propanediyl)bis(1,1-diphenylphosphine-kappaP))nickelHCID 2724937—
용매TetrahydrofuranHCID 8028—
생성물6-Ethyl-3,5-dimethoxy-pyridine-2-carbonitrileHCID 66986777—

반응 조건

온도0 °C

반응 단계

Impure 6-bromo-3,5-dimethoxy-pyridine-2-carbonitrile (462 mg; <1.9 mmol) was dissolved in tetrahydrofuran (20 mL) under nitrogen, and to the solution was added 1,3-bis(diphenylphosphino)propane nickel (II) chloride (105 mg; 0.19 mmol). The solution was cooled to 0° C., and a solution of ethyl magnesium bromide (1.0 molar in THF; 2.7 mL; 1.4 eq.) was slowly added. The reaction was stirred for five minutes, and quenched with saturated aqueous ammonium chloride (10 mL). To the reaction was added ethyl acetate (40 mL) and water (40 mL). The organic layer was isolated, dried over sodium sulfate, evaporated, and purified by column chromatography to give 6-ethyl-3,5-dimethoxy-pyridine-2-carbonitrile (114 mg; 0.6 mmol).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835464B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-532f1d6b6fa349359073f09aec098b3b
출처 메모uspto-grants-2014_09