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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 33999생성일: 2026년 10월 26일

Ammonium Chloride → (3-Fluorophenyl)-(3-fluoropyridin-2-yl)-methanol

https://huagongshe.com/reaction/33999

반응식

참여 물질

역할이름HCID투입량
반응물Ammonium ChlorideHCID 25517—
반응물3-FluoropyridineHCID 67794—
반응물3-FluorobenzaldehydeHCID 68009—
반응물ButyllithiumHCID 178418339—
용매Diethyl EtherHCID 3283—
용매HexaneHCID 8058—
용매Ethyl AcetateHCID 8857—
생성물(3-Fluorophenyl)-(3-fluoropyridin-2-yl)-methanolHCID 23070231—

반응 조건

온도-20 °C

반응 단계

Under nitrogen atmosphere, a solution of 9.75 g of diazabicyclo[2.2.0]octane in 150 mL of dehydrated diethyl ether was cooled to −40° C., added with 56 mL of 1.56 M n-butyllithium in hexane, and stirred at −20° C. for 1 hour. The solution was cooled to-60° C., added dropwise with 6.9 mL of 3-fluoropyridine, stirred at −60° C. for 1 hour, and added with 9.2 mL of 3-fluorobenzaldehyde. After stirring for 1 hour, aqueous ammonium chloride and ethyl acetate were successively added, and the mixture was recovered to room temperature. The organic layer was extracted, washed with water, and then dried over anhydrous magnesium sulfate. The solvent was evaporated, and the resulting crude product was purified and separated by silica gel column chromatography (ethyl acetate:hexane=1:4), to give 12.6 g of the title compound as colorless needle crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07429609B2
출처 데이터셋uspto-grants-2008_09
ORD IDord-301457584e034ef78be9b798feba0750
출처 메모uspto-grants-2008_09