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HRID 376515作成日:2026年10月26日

Tetrafluorophthalonitrile → 2-Phenylpropionitrile

https://huagongshe.com/reaction/376515

反応式

関与物質

役割名称HCID仕込み量
反応物TetrafluorophthalonitrileHCID 74600—
反応物TetrafluoroisophthalonitrileHCID 608182—
反応物2,3,4,6-TetrafluorobenzonitrileHCID 22287549—
生成物2-PhenylpropionitrileHCID 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

DOI10.6084/m9.figshare.5104873.v1
特許番号US06020517
出典データセットuspto-grants-2000_02
ORD IDord-41e1ed2ba8da46c882cfa7d1e54ed6d9
出典メモuspto-grants-2000_02