참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Chlorotoluene | HCID 7810 | — |
| 반응물 | Cesium fluoride | HCID 25953 | — |
| 반응물 | 1,4-Dioxane | HCID 31275 | — |
| 반응물 | HCID 178419127 | HCID 178419127 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 촉매 | 2,2'-Bis(dicyclohexylphosphino)-1,1'-binaphthyl | HCID 4368621 | — |
| 생성물 | 4-Methylbiphenyl | HCID 12566 | 93% |
반응 단계
An oven dried resealable Schlenk tube was purged with argon and charged with palladium acetate (4.4 mg, 0.02 mmol, 2 mol %), ligand 2 [Example 1] (11.9 mg, 0.03 mmol, 3 mol %), phenylboron dihydroxide (183 mg, 1.5 mmol), and cesium fluoride (456 mg, 3.0 mmol). The tube was purged with argon, and dioxane (3 mL) and 4-chlorotoluene (0.12 mL, 1.0 mmol) were added through a rubber septum. The septum was removed, the tube was sealed with a teflon screw cap and the mixture was stirred at room temperature until the starting aryl chloride had been completely consumed as judged by GC analysis. The reaction mixture was then diluted with ether (20 mL) and poured into a separatory funnel. The mixture was washed with 1M NaOH (20 mL), and the layers were separated. The aqueous layer was extracted with ether (20 mL), and the combined organic extracts were dried over anhydrous magnesium sulfate, filtered, and concentrated in vacuo. The crude material was then purified by flash chromatography on silica gel to give 157 mg (93%) of a glassy solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US07560582B2 |
|---|
| 출처 데이터셋 | uspto-grants-2009_07 |
|---|
| ORD ID | ord-a7e18cfdb83e4d6996b0398a3246b81a |
|---|
| 출처 메모 | uspto-grants-2009_07 |
|---|