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Tert-butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate → tert-Butyl 3-(2-oxoethyl)piperidine-1-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tert-butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate | HCID 69249758 | — |
| 溶媒 | Formic Acid | HCID 284 | — |
| 生成物 | tert-Butyl 3-(2-oxoethyl)piperidine-1-carboxylate | HCID 22258947 | 60% |
反応手順
tert-Butyl 3-(2-methoxyethenyl)-1-piperidinecarboxylate (1.16 g, 4.81 mmol) was dissolved in 90% formic acid (2 mL). The mixture was stirred at room temperature for 40 min. The mixture was then partitioned between ethyl acetate and saturated aqueous NaHCO3 solution. The separated organic phase was washed with brine, dried over Na2SO4, filtered and evaporated. Purification by column chromatography (hexane/ethyl acetate=4/1) gave tert-butyl 3-(2-oxoethyl)-1-piperidinecarboxylate as a colorless oil (652 mg, yield; 60%). [Starting Compound 2H]
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06984649B1 |
| 出典データセット | uspto-grants-2006_01 |
| ORD ID | ord-dfa4cf42235448b9bb08d335f6b60f00 |
| 出典メモ | uspto-grants-2006_01 |