돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 70516생성일: 2026년 10월 23일

Cyclopropylbenzene → (5-Chloro-6-methoxypyridin-2-yl)(4-cyclopropylphenyl)methanol

https://huagongshe.com/ko/reaction/70516

반응식

참여 물질

역할이름HCID투입량
반응물CyclopropylbenzeneHCID 70112—
반응물1-Bromo-4-cyclopropylbenzeneHCID 12221355—
반응물5-Chloro-6-methoxypicolinaldehydeHCID 58452846—
반응물ButyllithiumHCID 178418339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(5-Chloro-6-methoxypyridin-2-yl)(4-cyclopropylphenyl)methanolHCID 67399283—

반응 단계

n-Butyllithium (1.65 M, 3 mL) was added dropwise to a solution of the mixture of 4-bromo-1-cyclopropylbenzene and cyclopropylbenzene (976 mg) in tetrahydrofuran (20 mL) at −78° C. in a nitrogen atmosphere, and the mixture was stirred at the same temperature for 30 minutes. A solution of 5-chloro-6-methoxypyridine-2-carbaldehyde (732 mg) in tetrahydrofuran (9 mL) was added to the reaction solution at −78° C., and the mixture was stirred at the same temperature for three hours. Water was added to the reaction solution, followed by extraction with ethyl acetate. The organic layer was washed with brine, dried over anhydrous magnesium sulfate and filtered. The solvent was then evaporated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane:ethyl acetate=100:0→1:10) to give (5-chloro-6-methoxypyridin-2-yl)(4-cyclopropylphenyl)methanol (765 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08822503B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-1fec8c23d92843c58147f70a2606c192
출처 메모uspto-grants-2014_09