関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | N,N,N',N'-Tetramethylethylenediamine | HCID 8037 | — |
| 反応物 | 1-Benzyl-4-piperidone | HCID 19220 | — |
| 反応物 | 2,3-Dihydro-2,2-dimethylbenzofuran | HCID 80640 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 溶媒 | Heptane | HCID 8900 | — |
| 生成物 | HCID 23282674 | HCID 23282674 | 19.3% |
反応手順
A mixture of 2,3-dihydro-2,2-dimethylbenzofuran (25 g) and tetramethylethylenediamine (46 g) in heptane (250 ml) was treated dropwise at room temperature with 1.6 M BuLi in hexane (250 ml). After stirring for 1.5 h at 30-40° C. the mixture was cooled to -40° C. and 1-benzyl-4-piperidinone (32 g) was added dropwise at -40° C. The reaction mixture was allowed to warm to room temperature during 3 h followed by quench with water. After concentrating the reaction mixture in vacuo dichloromethane (500 ml) was added followed by wash with water (3×500 ml). Removal of solvent in vacuo gave an oil which was purified by flash chromatography (silica gel, heptane/ethyl acetate/triethylamine 50:48:2) giving an oil. Addition of heptane gave the product, 7-(1-benzyl-4-hydroxy-4-piperidinyl)-2,3-dihydro-2,2-dimethylbenzofuran as a solid (11 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06140331 |
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| 出典データセット | uspto-grants-2000_10 |
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| ORD ID | ord-473a973c775e47bfa3c6acd82b096acc |
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| 出典メモ | uspto-grants-2000_10 |
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