関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Dimethyl Sulfoxide | HCID 679 | — |
| 反応物 | Cesium carbonate | HCID 10796 | — |
| 反応物 | 4-Chloro-3-nitrobenzaldehyde | HCID 85505 | — |
| 反応物 | Methyl isonipecotate | HCID 424914 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | Methyl 1-(4-formyl-2-nitrophenyl)piperidine-4-carboxylate | HCID 9111291 | 43.7% |
反応手順
To a mixture of 4-chloro-3-nitrobenzaldehyde 57 (5.099 g, 27 mmol), cesium carbonate (9.48 g, 29 mmol), and methyl piperidine-4-carboxylate (4 mL, 27 mmol) was added DMSO (27 mL). The reaction mixture was heated to 100° C. for 30 min and diluted with EtOAc. The organic phase was washed with water (2×), brine (1×), dried over MgSO4, filtered, and concentrated in vacuo. Purification by flash column chromatography on silica gel (eluted with 30% to 50% EtOAc in hexanes) gave methyl 1-(4-formyl-2-nitrophenyl)piperidine-4-carboxylate 58 (3.45 g, 43% yield) as a yellow oil. Mass spectrum: calculated for C14H16N2O5 292.1. found 293.1 (M++1).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08349831B2 |
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| 出典データセット | uspto-grants-2013_01 |
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| ORD ID | ord-6a1c2fc5105048648d90d137b877ecb4 |
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| 出典メモ | uspto-grants-2013_01 |
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