戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 35024作成日:2026年10月27日

4-Aminophenethyl alcohol → 2,2,3,3,4,4,4-heptafluoro-N-[4-(2-hydroxyethyl)phenyl]butanamide

https://huagongshe.com/reaction/35024

反応式

関与物質

役割名称HCID仕込み量
反応物4-Aminophenethyl alcoholHCID 66904—
反応物Heptafluorobutyryl ChlorideHCID 67810—
反応物DiisopropylethylamineHCID 81531—
溶媒DichloromethaneHCID 6344—
生成物2,2,3,3,4,4,4-heptafluoro-N-[4-(2-hydroxyethyl)phenyl]butanamideHCID 2129770665.4%

反応手順

To a 0° C. solution of 2-[(4-amino)phenyl]ethanol (25 g), diisopropylethylamine (23.9 g) and dichloromethane (400 mL) was added heptafluorobutyryl chloride (41.8 g) dropwise over 0.5 hour. The mixture was allowed to warm gradually to room temperature and stirred for 2 hours. The precipitate was filtered off and the filtrate was diluted with ethylacetate (100 mL), washed with water (3×500 mL), dried over sodium sulfate, filtered and concentrated with a rotary evaporator. The residue was triturated with dichloromethane and collected by filtration. The combined solids were dissolved in diethyl ether and washed with water and saturated aqueous sodium chloride solutions, dried over sodium sulfate, filtered and concentrated to give 2,2,3,3,4,4,4-heptafluoro-N-[4-(2-hydroxyethyl)phenyl]butanamide as a white solid (39.2 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04764623
出典データセットuspto-grants-1988_08
ORD IDord-fa007ed498ef49a68d2ca58b8f6aa7cc
出典メモuspto-grants-1988_08