Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Dichloromethane → 2-Fluoro-6-octyloxy-3-[4-(4-octyloxyphenyl)phenyl]pyridine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Dichloromethane | HCID 6344 | — |
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | 1-Bromo-4-(4-octoxyphenyl)benzene | HCID 2801787 | — |
| 반응물 | 2-Fluoro-6-octyloxypyridine-3-boronic acid | HCID 19046940 | — |
| 촉매 | HCID 178418397 | HCID 178418397 | — |
| 용매 | Benzene | HCID 241 | — |
| 용매 | Ethanol | HCID 702 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 2-Fluoro-6-octyloxy-3-[4-(4-octyloxyphenyl)phenyl]pyridine | HCID 19046973 | 13.2% |
반응 단계
2.10 g (7.50 mmol) of 2-fluoro-6-octyloxypyridine-3-boronic acid (prepared as described in Example 5) in 35 ml of ethanol are refluxed together with 2.70 g (7.50 mmol) of 4-bromo-4'-octyloxybiphenyl and 0.29 g (0.24 mmol) of tetrakis(triphenylphosphine)palladium in 46 ml of benzene and 2.5 g (23.40 mmol) of sodium carbonate in 11 ml of water for 20 hours. After distributing the reaction mixture between water and dichloromethane, the organic phase is washed with sodium chloride solution, dried over sodium sulfate, filtered and concentrated. Purification of the residue by chromatography (silica gel, dichloromethane) and recrystallization from acetonitrile give 0.50 g of 2-fluoro-6-octyloxy-3-[4-(4-octyloxyphenyl)phenyl]pyridine. ##STR32##
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US05630962 |
| 출처 데이터셋 | uspto-grants-1997_05 |
| ORD ID | ord-51874d2e1e3549caa257c4049dcb364b |
| 출처 메모 | uspto-grants-1997_05 |