関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Benzene, 1,3-dichloro-5-nitro- | HCID 12064 | — |
| 反応物 | Potassium Hydroxide | HCID 14797 | — |
| 反応物 | 2-DI-Tert-Butylphosphino-2,4,6-Triisopropylbiphenyl | HCID 66849835 | — |
| 触媒 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 溶媒 | Water | HCID 962 | — |
| 溶媒 | 1,4-Dioxane | HCID 31275 | — |
| 溶媒 | Water ethylacetate | HCID 22728543 | — |
| 生成物 | 3-Chloro-5-nitrophenol | HCID 10675815 | 67.8% |
反応手順
To a mixture of 1,3-dichloro-5-nitrobenzene (5.00 g, 26.0 mmol), potassium hydroxide (3.44 g, 52.1 mmol), tris(dibenzylideneacetone)dipalladium(0) (539 mg, 0.52 mmol), and 2-(di-tert-butylphosphino)-2,4,6-triisopropylbiphenyl (885 mg, 2.08 mmol) was added a degassed mixture of dioxane (25 mL) and water (15 mL). The mixture was heated for 30 min to 80° C., then diluted with water/ethyl acetate and acidified with diluted hydrochloric acid. The mixture was extracted three times with ethyl acetate. The combined organic layers were dried over sodium sulfate, and the solvent was removed in vacuo. The crude product was purified by column chromatography on silica gel (eluent: cyclohexane/ethyl acetate 3:1). The product was then triturated with petroleum ether/tert-butyl methyl ether and collected by suction filtration to yield 3.06 g (66%) of the title compound as yellowish crystals.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08524722B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-6e688c6bb7214519b4f8e556437cacfe |
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| 出典メモ | uspto-grants-2013_09 |
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