関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Tributyltin Chloride | HCID 15096 | — |
| 反応物 | Lithium cyclohexylisopropylamide | HCID 10877271 | — |
| 反応物 | Phosphonic acid, 2-furanyl-, diethyl ester | HCID 12485182 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Diethyl 5-tributylstannyl-2-furanphosphonate | HCID 22280515 | — |
反応手順
A solution of diethyl 2-furanphosphonate (1 mmole, prepared as in Step C of Example 1) in THF was cooled at −78° C. and cannulated to a solution of lithium N-isopropyl-N-cyclohexylamide in THF at −78° C. over 15 min. The resulting mixture was stirred at −78° C. for 2 h and cannulated into a solution of tributyltin chloride (1 mmole) in THF at −78° C. over 20 min. The mixture was then stirred at −78° C. for 1 h, and at 25° C. for 12 h. Extraction and chromatography gave compound (14) as a light yellow oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06756360B1 |
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| 出典データセット | uspto-grants-2004_06 |
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| ORD ID | ord-ac6d7a8faf9d4c838dfacd28699a9e3f |
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| 出典メモ | uspto-grants-2004_06 |
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