関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Sulfuric Acid | HCID 1118 | — |
| 反応物 | Cyclohexylamine | HCID 7965 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | Diisobutylaluminum hydride | HCID 14487 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Cyclopropylacetonitrile | HCID 643447 | — |
| 溶媒 | Diethyl Ether | HCID 3283 | — |
| 溶媒 | Ethyl Acetate | HCID 8857 | — |
| 生成物 | N-(2-cyclopropylethylidene)cyclohexylamine | HCID 19067101 | — |
反応手順
To a solution of cyclopropylacetonitrile (7.0 ml, 82 mmol) in 200 ml of methylene chloride/hexanes (1:1) at -78° C. was added 90.0 ml of 1M DIBAL in hexanes (90 mmol) dropwise over 20 minutes. After complete addition, the solution was warmed to 0° C. and stirred for 2 hours. At this time, 140 ml of ethyl acetate was added at 0° C. and the solution warmed to room temperature. To the solution was added 140 ml of saturated NH4Cl and 250 ml of 1N H2SO4. The mixture was diluted with ether and shaken vigorously until the organic layer became clear. The organic layer was then washed with saturated NaHCO3. To this crude aldehyde solution was added 55 g of K2CO3 and 9.4 ml of cyclohexylamine (82 mmol) at room temperature and the reaction stirred for 48 hours. The reaction was filtered and evaporated and the residue distilled under reduced pressure to give the title compound. MS 166 (M+H)+ ; 1H NMR (CDCl3) δ0.12-0.19 (m, 2H), 0.46-0.53 (m, 2H), 0.76-0.91 (m, 1H), 0.95-1.90 (m, 10H) , 2.12 (dd, 2H, J=5.2 Hz, J=7.4 Hz), 2.93 (m, 1H), 7.71 (t, 1H, J=5.1 Hz).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05789591 |
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| 出典データセット | uspto-grants-1998_08 |
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| ORD ID | ord-5d7e661878ef46dba81c8c2cd4bbc194 |
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| 出典メモ | uspto-grants-1998_08 |
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