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ethyl N-(2-phenoxyethyl)piperidine-3-carboxylate → N-(2-phenoxyethyl)piperidine-3-carbaldehyde
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | ethyl N-(2-phenoxyethyl)piperidine-3-carboxylate | HCID 19085394 | — |
| 反応物 | Diisobutylaluminumhydride | HCID 21225700 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | N-(2-phenoxyethyl)piperidine-3-carbaldehyde | HCID 19085423 | — |
反応手順
Di-isobutylaluminium hydride (13.2 ml of 1.5M solution in toluene) was added to a mixture of ethyl N-(2-phenoxyethyl)piperidine-3-carboxylate (5.0 g) in dry THF (50 ml) at 0° C. under nitrogen with stirring. The mixture was quenched with water (5 ml) and then treated with saturated Rochelles salt solution. The mixture was stirred at room temperature for 30 minutes and then filtered. The filtrate was separated and the organic layer was washed, dried and evaporated to give N-(2-phenoxyethyl)piperidine-3-carbaldehyde as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05760035 |
| 出典データセット | uspto-grants-1998_06 |
| ORD ID | ord-86a32a8d7c7c4ddf816e1c1dd0855d91 |
| 出典メモ | uspto-grants-1998_06 |