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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 52754생성일: 2026년 10월 26일

Piperidine → 2,6-Di-tert-butyl-4-[4-cyano-alpha-(piperidin-1-yl)benzyl]phenol

https://huagongshe.com/reaction/52754

반응식

참여 물질

역할이름HCID투입량
반응물PiperidineHCID 8082—
반응물2,6-Di-tert-butylphenolHCID 31405—
반응물4-CyanobenzaldehydeHCID 66042—
용매O-XyleneHCID 7237—
생성물2,6-Di-tert-butyl-4-[4-cyano-alpha-(piperidin-1-yl)benzyl]phenolHCID 19963868—

반응 단계

2,6-Di-tert-butylphenol (4.12 g, 0.02 mol), 2.62 g (0.02 mol) of 4-cyano-benzaldehyde and 1.7 g (0.02 mol) of piperidine are refluxed under nitrogen in 25 ml of xylene for 24 hours. The solution is then evaporated in vacuo and the residue chromatographed on silica gel with toluene/ethyl acetate (9:1) to give 6.2 g of a practically pure title compound. A 5 g portion of said compound is recrystallized twice from acetonitrile to give 1.0 g of a pure sample as colorless crystals, melting at 139°-140° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05616774
출처 데이터셋uspto-grants-1997_04
ORD IDord-beda6d3011e24f9086c71fc392715617
출처 메모uspto-grants-1997_04