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HRID 35024Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/35024

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Aminophenethyl alcoholHCID 66904—
EduktHeptafluorobutyryl ChlorideHCID 67810—
EduktDiisopropylethylamineHCID 81531—
LösungsmittelDichloromethaneHCID 6344—
Produkt2,2,3,3,4,4,4-heptafluoro-N-[4-(2-hydroxyethyl)phenyl]butanamideHCID 2129770665,4%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04764623
Quelldatensatzuspto-grants-1988_08
ORD IDord-fa007ed498ef49a68d2ca58b8f6aa7cc
Quellennotizuspto-grants-1988_08