関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Aniline | HCID 6115 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | Benzene, 1-bromo-3-methyl-2-nitro- | HCID 142929 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 触媒 | Binap, (A+-)- | HCID 634876 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | (3-Methyl-2-nitrophenyl)phenylamine | HCID 10704534 | 88.1% |
反応手順
A mixture of 1-bromo-3-methyl-2-nitrobenzene (1 g, 4.63 mmol), phenylamine (422 μL, 4.63 mmol), Cs2CO3 (2.11 g, 6.48 mmol) and (R)-BINAP (5 mol %, 143 mg, 0.23 mmol) in toluene (20 mL) was degassed with a stream of nitrogen prior to addition of Pd(OAc)2 (25 mg, 0.11 mmol) and was stirred at 110° C. under a nitrogen atmosphere for 18 h. After cooling to RT, the mixture was partitioned between EtOAc and water. The organic layer was washed with brine, then dried (Na2SO4) and concentrated in vacuo. The resulting residue was purified by column chromatography (Si—PCC, gradient 0-35% DCM in cyclohexane) affording (3-Methyl-2-nitrophenyl)phenylamine as a red oil (931 mg, 88%). LCMS: RT 3.97 min [M+H]+ 229.1.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08653089B2 |
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| 出典データセット | uspto-grants-2014_02 |
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| ORD ID | ord-6970c8b8c212497992ab4d54a1cb1d73 |
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| 出典メモ | uspto-grants-2014_02 |
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