Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Tributylphosphine → HCID 21867689, 화합물
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Tributylphosphine | HCID 13831 | — |
| 반응물 | 3,4-Dimethoxyphenol | HCID 16251 | — |
| 반응물 | 1,1'-(Azodicarbonyl)dipiperidine | HCID 73042 | — |
| 반응물 | 4-(1-Hydroxy-3-butenyl)benzonitrile | HCID 11019345 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | HCID 21867689 | HCID 21867689 | 68.6% |
반응 단계
A cooled (0° C.) mixture of 4-(1-hydroxy-3-butenyl)benzonitrile (14.6 g, 84.3 mmol) and 3,4-dimethoxyphenol (19.5 g, 125.4 mmol) in toluene (500 mL) was treated with tributylphosphine (32.14 mL of 97% purity, 25.6 g, 126.4 mmol), followed by 1,1′-(azodicarbonyl)dipiperidine (31.8 g, 126.4 mmol). After addition was complete, the reaction mixture thickened and the temperature rose to 15° C. Additional toluene was added (500 mL), and the mixture stirred at rt overnight. The precipitate of tributylphosphine oxide was then removed by filtration and the filtrate concentrated in vacuo to give 65.8 g of crude product. This was purified by chromatography on silica gel, eluting with toluene:methanol (98:2), to yield 17.9 g of the sub-title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06559143B1 |
| 출처 데이터셋 | uspto-grants-2003_05 |
| ORD ID | ord-88a33979ca2345679982399a6e5a2de6 |
| 출처 메모 | uspto-grants-2003_05 |