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HRID 1780560생성일: 2026년 10월 27일

Dichloromethane → 1,4-Di(2-fluoro-6-octyloxypyridine-3-yl)benzene

https://huagongshe.com/reaction/1780560

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물1,4-DibromobenzeneHCID 7804—
반응물Sodium CarbonateHCID 10340—
반응물2-Fluoro-6-octyloxypyridine-3-boronic acidHCID 19046940—
촉매HCID 178418397HCID 178418397—
용매BenzeneHCID 241—
용매EthanolHCID 702—
용매WaterHCID 962—
생성물1,4-Di(2-fluoro-6-octyloxypyridine-3-yl)benzeneHCID 1904694779.8%

반응 단계

0.87 g (3.7 mmol) of 1,4-dibromobenzene, 2.00 g (7.4 mmol) of 2-fluoro-6-octyloxypyridin-3-boronic acid (prepared as described in Example 5), 0.56 g (0.46 mmol) of tetrakis(triphenylphosphine)palladium(0) and 5 g (46.1 mmol) of sodium carbonate in 50 ml of benzene, 35 ml of ethanol and 20 ml of water are refluxed for 18 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, CH2Cl2) and recrystallization from acetonitrile give 1.55 g of 1,4-di(2-fluoro-6-octyloxypyridine-3-yl)benzene. ##STR36##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05630962
출처 데이터셋uspto-grants-1997_05
ORD IDord-a15a2e58252f4142aacc79a69cef98ad
출처 메모uspto-grants-1997_05