関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Diisopropylamine | HCID 7912 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Cyanocyclohexane | HCID 69834 | — |
| 反応物 | (Phenylmethoxy)acetaldehyde | HCID 108989 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Lithium diisopropylamide | HCID 2724682 | — |
| 生成物 | 1-(2-Benzyloxy-1-hydroxy-ethyl)-cyclohexanecarbonitrile | HCID 18388337 | 73% |
反応手順
Lithium diisopropylamide was prepared by dropwise addition of n-BuLi (2.03 mL; 2.5 M in Hexanes; 5.08 mmol) to a stirred and cooled (−10° C.) solution of i-Pr2NH (0.84 mL; 6.0 mmol) in dry tetrahydrofuran (40 mL). Stirring was continued for 20 minutes. The mixture was cooled to −78° C. and cyclohexane carbonitrile 1 (500 mg; 4.62 mmol) was added over 5 minutes. After a further 30 minutes, benzyloxyacetaldehyde (0.97 mL; 6.93 mmol) was added dropwise. Stirring was continued at −78° C. for 7 hours. The reaction mixture was then allowed to stir overnight at −20° C. Saturated aqueous NH4Cl was added (10 mL), and the mixture was extracted with diethyl ether (2×20° mL), dried over MgSO4 and evaporated. The residue was purified over silica gel chromatography (ether/heptane 1:1) to give 2 as a white solid (872 mg; 3.37 mmol; 73%)
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06316638B1 |
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| 出典データセット | uspto-grants-2001_11 |
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| ORD ID | ord-434f85a4ccee406586eef21d65f7b1b3 |
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| 出典メモ | uspto-grants-2001_11 |
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