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HRID 1780559생성일: 2026년 10월 27일

Dichloromethane → 2-Fluoro-6-octyloxy-3-[4-(4-octyloxyphenyl)phenyl]pyridine

https://huagongshe.com/reaction/1780559

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Sodium CarbonateHCID 10340—
반응물1-Bromo-4-(4-octoxyphenyl)benzeneHCID 2801787—
반응물2-Fluoro-6-octyloxypyridine-3-boronic acidHCID 19046940—
촉매HCID 178418397HCID 178418397—
용매BenzeneHCID 241—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물2-Fluoro-6-octyloxy-3-[4-(4-octyloxyphenyl)phenyl]pyridineHCID 1904697313.2%

반응 단계

2.10 g (7.50 mmol) of 2-fluoro-6-octyloxypyridine-3-boronic acid (prepared as described in Example 5) in 35 ml of ethanol are refluxed together with 2.70 g (7.50 mmol) of 4-bromo-4'-octyloxybiphenyl and 0.29 g (0.24 mmol) of tetrakis(triphenylphosphine)palladium in 46 ml of benzene and 2.5 g (23.40 mmol) of sodium carbonate in 11 ml of water for 20 hours. After distributing the reaction mixture between water and dichloromethane, the organic phase is washed with sodium chloride solution, dried over sodium sulfate, filtered and concentrated. Purification of the residue by chromatography (silica gel, dichloromethane) and recrystallization from acetonitrile give 0.50 g of 2-fluoro-6-octyloxy-3-[4-(4-octyloxyphenyl)phenyl]pyridine. ##STR32##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05630962
출처 데이터셋uspto-grants-1997_05
ORD IDord-51874d2e1e3549caa257c4049dcb364b
출처 메모uspto-grants-1997_05