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Benzene → Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Benzene | HCID 241 | — |
| 反応物 | Methyl vinyl ketone | HCID 6570 | — |
| 反応物 | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| 反応物 | Benzyl 4-formylpiperidine-1-carboxylate | HCID 2776272 | — |
| 生成物 | Benzyl 9-oxo-3-azaspiro(5.5)undec-7-ene-3-carboxylate | HCID 23435732 | 57.2% |
反応手順
Benzyl 4-formylpiperidine-1-carboxylate (5.17 g, 20.907 mmol) and p-Toluenesulfonic acid monohydrate (0.398 g, 2.091 mmol) were stirred in Benzene (30.0 ml, 334.136 mmol) at 70° C. But-3-en-2-one (3.76 ml, 41.813 mmol) was added and the reaction mixture was refluxed o/n while removing water with dean-stark trap. After cooling the reaction mixture to rt, sat. NaHCO3 soln. was added and the organic layer was dried over Na2SO4 and evaporated. The resulting oil was purified by Biotage (SiO2, 250 g, EtOAc/Hep 10% to 50%) to afford the title compound (3.58 g, 11.96 mmol, 57.2% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09446046B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-7f02d74748974695a9ee031a838a2b47 |
| 出典メモ | uspto-grants-2016_09 |