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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52755생성일: 2026년 10월 25일

4-(Dimethylamino)Benzaldehyde → 2,6-Di-tert-butyl-4-((4-(dimethylamino)phenyl)(piperidin-1-yl)methyl)phenol

https://huagongshe.com/reaction/52755

반응식

참여 물질

역할이름HCID투입량
반응물4-(Dimethylamino)BenzaldehydeHCID 7479—
반응물PiperidineHCID 8082—
반응물2,6-Di-tert-butylphenolHCID 31405—
반응물Toluene hexaneHCID 21889329—
용매O-XyleneHCID 7237—
생성물2,6-Di-tert-butyl-4-((4-(dimethylamino)phenyl)(piperidin-1-yl)methyl)phenolHCID 4066737—

반응 단계

To 30.4 g (0.2 mol) of 4-dimethylaminobenzaldehyde in 100 ml of xylene, 39.1 g (0.46 mol) of piperidine is added dropwise over a period of six minutes. The mixture is heated at reflux using a Dean-Stark trap until the separation of water is complete. To the cooled reaction mixture 40.3 (0.2 mol) of 2,6-di-tert-butylphenol in 70 ml of xylene is added rapidly. The mixture is then heated at reflux for five hours. The title compound is isolated as an almost white solid by evaporation of the solvent and recrystallization from toluene-hexane. The yield is 66.3 g of the title compound, melting at 184°-185° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616774
출처 데이터셋uspto-grants-1997_04
ORD IDord-beb031635aaa49749c8a2909d1afb736
출처 메모uspto-grants-1997_04