戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 548595作成日:2026年10月24日

p-Toluenesulfonic acid → HCID 57691414、化合物

https://huagongshe.com/ja/reaction/548595

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物2,5-HexanedioneHCID 8035—
反応物Phenylglycine nitrileHCID 76307—
触媒p-Toluenesulfonic acidHCID 6101—
溶媒TolueneHCID 1140—
生成物HCID 57691414HCID 57691414102.1%

反応条件

温度155 °C

反応手順

p-Toluenesulfonic acid (2 mg, 0.16 mmol) and acetonylacetone (2.14 g, 18.7 mmol) were added sequentially to a solution of 2-aminophenylacetonitrile (2.06 g, 15.6 mmol) in toluene (30 mL). The reaction mixture was heated in an oil bath at 155° C. for 1 hour and then allowed to stand at ambient temperature overnight. Acetonylacetone (0.5 mL) and a small amount of p-toluenesulfonic acid were added and the reaction mixture was heated at reflux for 4 hours. The toluene layer was washed sequentially with saturated sodium bicarbonate and water (×2), dried over magnesium sulfate, filtered, and then concentrated under reduced pressure to a dark oil. The oil was purified by prep HPLC (AnaLogix, eluted with a gradient of 10-30% ethyl acetate in hexanes) to provide 3.35 g of 2-(2,5-dimethylpyrrol-1-yl)phenylacetonitrile as a pale brown oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07943610B2
出典データセットuspto-grants-2011_05
ORD IDord-b40475f78fa44b38b242a1e3a0993b80
出典メモuspto-grants-2011_05