Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Acetone → 2-[3,5-Di(2-methylallyl)phenyl]oxazolo[4,5-b]pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Acetone | HCID 180 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | Phosphonium | HCID 5460504 | — |
| 반응물 | 2-[3,5-Bis(bromomethyl)phenyl][1,3]oxazolo[4,5-b]pyridine | HCID 22754828 | — |
| 반응물 | Lithium ethoxide | HCID 23661847 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2-[3,5-Di(2-methylallyl)phenyl]oxazolo[4,5-b]pyridine | HCID 22754778 | — |
반응 단계
A mixture of 5 mmoles of the product from Step A and 11.0 mmoles of triphenylphosphine in 15 ml. of dimethylformamide is stirred and refluxed under nitrogen for 3 hours. The mixture is cooled and the phosphonium salt is collected on a filter. A mixture of 4 mmoles of the phosphonium salt, 100 ml. of ethanol, 1 ml. of acetone and 40 ml. of 0.3 N ethanolic lithium ethoxide is stirred at room temperature under nitrogen for 2 hours. Water (100 ml.) is added and the mixture is cooled in an ice-bath. The precipitate is collected and purified by chromatography on silica gel using 2% methanol in chloroform as the eluant to give 2-[3,5-di(2-methylallyl)phenyl]oxazolo[4,5-b]pyridine.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US04131677 |
| 출처 데이터셋 | uspto-grants-1978_12 |
| ORD ID | ord-d3b0b6db65ed4ff39866941040eacc9e |
| 출처 메모 | uspto-grants-1978_12 |