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HRID 356825作成日:2026年10月26日

2-tert-Butyl-4-methylphenol → HCID 178426895、化合物

https://huagongshe.com/reaction/356825

反応式

関与物質

役割名称HCID仕込み量
反応物2-tert-Butyl-4-methylphenolHCID 17004—
反応物HCID 178418573HCID 178418573—
溶媒Diethyl EtherHCID 3283—
生成物HCID 178426895HCID 178426895—

反応条件

温度25 °C

反応手順

In an atmosphere of nitrogen, 3.29 g (20 mmol) of 2-tert-butyl-4-methylphenol was dissolved in 10 ml of diethyl ether and 6.7 ml of methylmagnesium bromide (20 mmol of diethyl ether solution) was added dropwise to this at 0° C. for 5 minutes. After completion of the dropwise addition, the reaction mixture was stirred at 25° C. for 10 minutes, subsequently, the diethyl ether was evaporated under vacuum, and 30 ml of toluene was added to-obtain a toluene solution of 2-tert-butyl-4-methylphenoxymagnesium bromide. To the solution, 1.07 g (10 mmol) of picolinaldehyde was added dropwise at 25° C. and it was reacted for 5 hours while refluxing. After cooling, the reaction was stopped by adding aqueous 5% hydrochloric acid solution and successively, after neutralizing it with aqueous sodium hydrogencarbonate solution, the organic layer obtained was washed with a saturated aqueous sodium chloride solution. After drying it over anhydrous magnesium sulfate, the solvent was distilled off. The residue was purified by silica gel column chromatography (a developing solvent: hexane/ethyl acetate=20/1-1/1) to obtain 2-bis(2-hydroxy-3-tert-butyl-5-methylphenyl)methylpyridine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05840646
出典データセットuspto-grants-1998_11
ORD IDord-fa8039eb9b6249ee858941d40643aea2
出典メモuspto-grants-1998_11