Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Piperidine → 2,6-Di-tert-butyl-4-[4-cyano-alpha-(piperidin-1-yl)benzyl]phenol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| 반응물 | 4-Cyanobenzaldehyde | HCID 66042 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 2,6-Di-tert-butyl-4-[4-cyano-alpha-(piperidin-1-yl)benzyl]phenol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05616774 |
| 출처 데이터셋 | uspto-grants-1997_04 |
| ORD ID | ord-beda6d3011e24f9086c71fc392715617 |
| 출처 메모 | uspto-grants-1997_04 |