Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
4-(Dimethylamino)Benzaldehyde → 2,6-Di-tert-butyl-4-((4-(dimethylamino)phenyl)(piperidin-1-yl)methyl)phenol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 4-(Dimethylamino)Benzaldehyde | HCID 7479 | — |
| 반응물 | Piperidine | HCID 8082 | — |
| 반응물 | 2,6-Di-tert-butylphenol | HCID 31405 | — |
| 반응물 | Toluene hexane | HCID 21889329 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | 2,6-Di-tert-butyl-4-((4-(dimethylamino)phenyl)(piperidin-1-yl)methyl)phenol | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05616774 |
| 출처 데이터셋 | uspto-grants-1997_04 |
| ORD ID | ord-beb031635aaa49749c8a2909d1afb736 |
| 출처 메모 | uspto-grants-1997_04 |