関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tributylamine | HCID 7622 | — |
| 反応物 | tert-Butyl acrylate | HCID 15458 | — |
| 反応物 | 1-(2-Bromo-4-chlorophenyl)ethanone | HCID 4712644 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 触媒 | palladium(II) acetate | HCID 167845 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (E)-tert-butyl 3-(2-acetyl-5-chlorophenyl)acrylate | HCID 89499883 | 63.2% |
反応手順
To a degassed solution of 1-(2-bromo-4-chlorophenyl)ethanone (1.0 g, 4.28 mmol), tributylamine (2.041 mL, 8.57 mmol), and tert-butyl acrylate (1.255 mL, 8.57 mmol) in DMF (10 mL) was added palladium on carbon (0.456 g, 0.428 mmol) and Pd(OAc)2 (0.096 g, 0.428 mmol). The reaction mixture was warmed to 100° C. After 16 h, the reaction was cooled to rt. The reaction was filtered and the solid was rinsed with DMF. The filtrate was diluted with EtOAc, washed with H2O (2×), brine, dried over Na2SO4, filtered and concentrated. Purification by normal phase chromatography afforded Intermediate 4A (0.760 g, 63%), as a brown oil. MS (ESI) m/z: 225.0 (M-C4H8+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09108951B2 |
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| 出典データセット | uspto-grants-2015_08 |
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| ORD ID | ord-e6109ceab95f42b99835a4e040a87c59 |
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| 出典メモ | uspto-grants-2015_08 |
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