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HRID 443766作成日:2026年10月26日

O-Xylene → 2-(1,8,8-Trimethyl-3-azabicyclo[3.2.1]octyl)-4,6-bis(1,1,2,2-tetramethylpropylamino)-s-triazine

https://huagongshe.com/reaction/443766

反応式

関与物質

役割名称HCID仕込み量
反応物O-XyleneHCID 7237—
反応物DiisopropylethylamineHCID 81531—
反応物3-Azabicyclo[3.2.1]octane, 1,8,8-trimethyl-, (+)-HCID 536556—
反応物2-Chloro-4,6-di(2,3,3-trimethyl-2-butyl)amino-s-triazineHCID 15572577—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒Ethyl AcetateHCID 8857—
生成物2-(1,8,8-Trimethyl-3-azabicyclo[3.2.1]octyl)-4,6-bis(1,1,2,2-tetramethylpropylamino)-s-triazineHCID 70562567—

反応手順

Seven grams (0.02 mole) of 2-chloro-4,6-bis[(1,1,2,2-tetramethylpropyl)amino]-s-triazine, 31 g. (0.2 mole) of 1,8,8-trimethyl-3-azabicyclo[3.2.1]octane, 7.1 ml. (0.04 mole) of N,N-diisopropylethylamine and xylene are refluxed under an argon atmosphere for 22 hours. After cooling, the reaction is diluted with ethyl acetate and water. The mixture is then washed with water, the organic phase dried over magnesium sulfate, filtered through diatomaceous earth and evaporated in vacuo. Addition of toluene and re-evaporation in vacuo several times gives a solid. This solid is then dissolved in dichloromethane, filtered through Magnesol® and the Magnesol® washed with dichloromethane. Evaporation of the solvent and purification by column chromatography gives 2-(1,8,8-trimethyl-3-azabicyclo[3.2.1]octyl)-4,6-bis(1,1,2,2-tetramethylpropylamino)-s-triazine.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04261892
出典データセットuspto-grants-1981_04
ORD IDord-796f72c0aa804be1beb5a1237ed4953f
出典メモuspto-grants-1981_04