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HRID 1780067作成日:2026年10月27日

Ethanol → 3-Chloro-2,5-di(4-octyloxyphenyl)pyridine

https://huagongshe.com/reaction/1780067

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium CarbonateHCID 10340—
反応物4-n-Octyloxyphenylboronic Acid (contains varying amounts of Anhydride)HCID 3977284—
反応物5-Bromo-3-chloro-2-(4-octyloxyphenyl)pyridineHCID 19050004—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物3-Chloro-2,5-di(4-octyloxyphenyl)pyridineHCID 1904999348.9%

反応手順

2.00 g (5.40 mmol) of 5-bromo-3-chloro-2-(4-octyloxyphenyl)pyridine, 1.50 g (6.00 mmol) of 4-octyloxybenzeneboronic acid, 0.07 g (0.6 mmol) of tetrakis(triphenylphosphine)palladium(0) and 1.3 g (12.00 mmol) of sodium carbonate are heated at 80° C. for 3 hours in 20 ml of toluene, 10 ml of ethanol and 10 ml of water. The mixture is subsequently partitioned between aqueous sodium chloride solution and ether, the organic phase is washed with aqueous sodium chloride solution, dried over sodium sulfate and evaporated, and the product is purified by chromatography (silica gel/dichloromethane), giving 1.38 g of 3-chloro-2,5-di(4-octyloxyphenyl)pyridine. ##STR24##

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05629428
出典データセットuspto-grants-1997_05
ORD IDord-6369c675c53c486b9e2852c43191dc58
出典メモuspto-grants-1997_05