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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 396732생성일: 2026년 10월 23일

N,N-Dimethylbenzylamine → 2-[2-Hydroxy4(3-butoxy-2-hydroxypropyloxy)-phenyl]4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin

https://huagongshe.com/ko/reaction/396732

반응식

참여 물질

역할이름HCID투입량
반응물N,N-DimethylbenzylamineHCID 7681—
반응물Butyl glycidyl etherHCID 17049—
반응물2-(2,4-Dihydroxyphenyl)-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazineHCID 74276—
용매O-XyleneHCID 7237—
생성물2-[2-Hydroxy4(3-butoxy-2-hydroxypropyloxy)-phenyl]4,6-bis(2,4-dimethylphenyl)-1,3,5-triazinHCID 13560141286%

반응 단계

23.8 g (0.06 mol) of 2-(2,4-dihydroxyphenyl)-4,6-bis-(2,4-dimethylphenyl)-1,3,5-triazine (prepared as described in U.S. Pat. No. 3,244,708 Example 16) are suspended in 300 ml of xylene. 12.1 g (0.09 mol) of 97% butyl glycidyl ether and 0.75 g (0.006 mol) of dimethylbenzylamine are added to this suspension, and the mixture is heated to reflux temperature. After a reaction time of 5 hours the clear, brownish solution is cooled and clarified by filtration through 100 g of silica gel. The yellow solution is evaporated and the residue is recrystallized from hexane/toluene. This gives 27.3 g of pale yellow crystals of 2-[2-hydroxy-4(3-butoxy-2-hydroxypropyloxy)-phenyl]-4,6-bis(2,4-dimethylphenyl)-1,3,5-triazin (=86% yield). Melting point: 80-83° C. (Compound 1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06608122B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-89f6527309c7417da998df8ccd1ab7c7
출처 메모uspto-grants-2003_08