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Tetrafluorophthalonitrile → 2-Phenylpropionitrile
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Tetrafluorophthalonitrile | HCID 74600 | — |
| 反応物 | Tetrafluoroisophthalonitrile | HCID 608182 | — |
| 反応物 | 2,3,4,6-Tetrafluorobenzonitrile | HCID 22287549 | — |
| 生成物 | 2-Phenylpropionitrile | HCID 15761 | — |
反応手順
By a method similar to Example 11, a reaction was carried out using 2,4,5,6-tetrafluoroisophthalonitrile, instead of 3,4,5,6-tetrafluorophthalonitrile. After 5 hours, the reaction solution was analyzed by gas chromatography, whereupon the conversion of 2,4,5,6-tetrafluoroisophthalonitrile was found to be 36% and the yield of 2,3,4,6-tetrafluorobenzonitrile (based on 2,4,5,6-tetrafluoroisophthalonitrile) was 20%. At the same time, 1.1 mmol of α-methylbenzylcyanide was produced. This corresponded to 0.35 times molar amount relative to the production of 2,3,4,6-tetrafluorobenzonitrile.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06020517 |
| 出典データセット | uspto-grants-2000_02 |
| ORD ID | ord-41e1ed2ba8da46c882cfa7d1e54ed6d9 |
| 出典メモ | uspto-grants-2000_02 |