関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | HCID 178418348 | HCID 178418348 | — |
| 反応物 | HCID 178445862 | HCID 178445862 | — |
| 反応物 | HCID 178509802 | HCID 178509802 | — |
| 触媒 | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Hexane | HCID 8058 | — |
| 生成物 | HCID 178443899 | HCID 178443899 | 118.8% |
反応手順
A mixture of 705 mg of dry copper-(I) iodide and 7 ml of tetrahydrofuran was treated dropwise with 2.5 ml of a 1.5M solution of methyl lithium in hexane at -78° C. while stirring vigorously and then warmed slowly to 0° C. Subsequently, the mixture was again cooled to -78° C. and treated dropwise by means of a syringe with a 4-pentenyl-magnesium bromide solution (prepared from 90 mg of magnesium and 0.44 ml of 5-bromo-1-pentene in 2 ml of tetrahydrofuran). The reaction mixture was warmed gradually until a red-violet suspension had formed and was then held at 5° C. for 20 minutes. Thereafter, the reaction mixture was again cooled to -78° C., treated dropwise with a solution of 600 mg of trans-4-(p-cyanophenyl)-iodomethylcyclohexane in 5 ml of tetrahydrofuran and then warmed slowly to room temperature. The reaction mixture was stirred at room temperature for a further 30 minutes and then treated with saturated ammonium chloride solution and extracted with diethyl ether. The organic phases were dried over magnesium sulphate and concentrated. Chromatographic separation on silica gel with ethyl acetate/petroleum ether (vol. 5:95) and two-fold recrystallization from methanol gave 165 mg of p-[trans-4-(5-hexenyl)cyclohexyl]benzonitrile (purity 99.75%) as colourless crystals of m.p. (C-N) 45.5° C. and cl.p. (N-I) 52.5° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US04770503 |
|---|
| 出典データセット | uspto-grants-1988_09 |
|---|
| ORD ID | ord-3ff8eb09d695430bb02b86f1c1599b49 |
|---|
| 出典メモ | uspto-grants-1988_09 |
|---|