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Acetonitrile → Methyl (RS)-4-cyano-2-phenylbutanoate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Acetonitrile | HCID 6342 | — |
| 反応物 | Ammonium Chloride | HCID 25517 | — |
| 反応物 | Methyl atropate | HCID 193334 | — |
| 反応物 | Lithium diisopropylamide | HCID 2724682 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 溶媒 | Cyclohexane | HCID 8078 | — |
| 生成物 | Methyl (RS)-4-cyano-2-phenylbutanoate | HCID 53645094 | 75% |
反応手順
Lithium diisopropylamide (3.67 ml of a 1.5 molar solution in cyclohexane) was added to acetonitrile (0.26 ml) in tetrahydrofuran (10 ml) at -78° C. After 1 hour, methyl 2-phenyl-acrylate (see Preparation 22) (0.81 g) in tetrahydrofurn (10 ml) was added and the mixture was stirred for 1 hour, allowed to warm to room temperature then treated with saturated ammonium chloride solution. The resulting mixture was partitioned between ethyl acetate and water, the organic phase dried over magnesium sulphate and evaporated to give a residue which was partitioned between ether and 10% aqueous sodium carbonate. The organic layer was dried over magnesium sulphate and evaporated to leave the title compound (0.5 g, 75%) as an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05292749 |
| 出典データセット | uspto-grants-1994_03 |
| ORD ID | ord-80af75f55504407f8422051aeb00f6fc |
| 出典メモ | uspto-grants-1994_03 |