関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 反応物 | 1-Bromo-3-(trifluoromethoxy)benzene | HCID 519964 | — |
| 反応物 | 2-Bromo-5-methylpyridine | HCID 564216 | — |
| 反応物 | HCID 178418306 | HCID 178418306 | — |
| 触媒 | Zincchloride | HCID 3007855 | — |
| 触媒 | Nickel--triphenylphosphane (1/2) | HCID 57357981 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Pentane | HCID 8003 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 2-(3-Trifluoromethoxyphenyl)-5-methylpyridine | HCID 54520146 | — |
反応手順
To a solution of 3-bromotrifluoromethoxybenzene (0.590 mL, 4.00 mmol) in THF (12 mL) at -78° C. was added t-butyl lithium (4.71 mL, of a 1.7M solution in pentane, 8.00 mmol. After 10 minutes zinc chloride(4.0 mL, of a 1M solution in diethylether, 4.00 mmol) was added. The reaction was stirred for 10 minutes at -78° C. and then allowed to warm to 0° C. and stirred for 30 minutes. This solution was added via cannula to a solution of 2-bromo-5-methyl pyridine and bis(triphenylphosphine) Nickel II chloride. The reaction stirred for 1 hour at 0° C. and then at ambient temperature for a furthur 1 hour. Saturated ammonium hydroxide solution (3 mL) was added and the mixture stirred until homogenous, extracted with Et2O and the organic extracts washed with saturated brine, dried (MgSO4) and evaporated in vacuo. The residue was chromatographed (Silica gel, 25-50% CH2Cl2 in hexanes).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05872136 |
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| 出典データセット | uspto-grants-1999_02 |
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| ORD ID | ord-89439644dad44269915f26bafa0e3617 |
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| 出典メモ | uspto-grants-1999_02 |
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