関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydracrylonitrile | HCID 8011 | — |
| 反応物 | 1,1-Cyclohexanediacetic Anhydride | HCID 2734289 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | 1-[(2-Cyanoethoxycarbonyl)methyl]-1-Cyclohexane Acetic Acid | HCID 22340960 | 95% |
反応手順
8.2 mL of 1.6M butyllithium was added to a −78° C. solution of 3-hydroxy-propionitrile (13.19 mmol) in 50 mL of THF. The reaction mixture was warmed to 30° C. and stirred for 30 minutes. Then, a solution of 1,1-cyclohexanediacetic anhydride (10.99 mmol) in 10 mL of THF was added dropwise. The reaction mixture was warmed to room temperature over a period of one hour and stirred at room temperature with monitoring by TLC. When the reaction was judged complete, the reaction mixture was quenched with saturated ammonium chloride solution and THF was removed under reduced pressure. The aqueous layer was extracted with ethyl acetate, washed with brine and dried over Na2SO4. After concentration in vacuo the residue was purified on silica gel (5% methanol in dichloromethane) to afford 2.64 g (95%) of the title compound. 1H NMR (CDCl3): δ 4.28 (2H, t, J=6.4 Hz); 2.71 (2H, t, J=6.4 Hz); 2.61 (4H, m); 1.52-1.42 (10H, m).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08143437B2 |
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| 出典データセット | uspto-grants-2012_03 |
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| ORD ID | ord-7832593f915c431eb735f2f2aafe911a |
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| 出典メモ | uspto-grants-2012_03 |
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