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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 443766생성일: 2026년 10월 25일

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

반응식

참여 물질

역할이름HCID투입량
반응물O-XyleneHCID 7237—
반응물DiisopropylethylamineHCID 81531—
반응물3-Azabicyclo[3.2.1]octane, 1,8,8-trimethyl-, (+)-HCID 536556—
반응물2-Chloro-4,6-di(2,3,3-trimethyl-2-butyl)amino-s-triazineHCID 15572577—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매Ethyl AcetateHCID 8857—
생성물2-(1,8,8-Trimethyl-3-azabicyclo[3.2.1]octyl)-4,6-bis(1,1,2,2-tetramethylpropylamino)-s-triazineHCID 70562567—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04261892
출처 데이터셋uspto-grants-1981_04
ORD IDord-796f72c0aa804be1beb5a1237ed4953f
출처 메모uspto-grants-1981_04