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HRID 1494446Erstellt: 24. Oktober 2026

Butyl bromide → N-butyl-N-acetyl-2,4-difluoroaniline

https://huagongshe.com/de/reaction/1494446

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktButyl bromideHCID 8002—
EduktPotassium HydroxideHCID 14797—
EduktAcetamide, N-(2,4-difluorophenyl)-HCID 96093—
KatalysatorBenzyl triethylammonium chlorideHCID 66133—
LösungsmittelWaterHCID 962—
LösungsmittelTolueneHCID 1140—
ProduktN-butyl-N-acetyl-2,4-difluoroanilineHCID 1982754968,7%

Reaktionsschritte

0.9 g of triethylbenzylammonium chloride, 6.9 g of butyl bromide and a solution of 5.7 g of KOH in 6 ml of water are added to a stirred solution of 3.4 g of N-acetyl-2,4-difluoroaniline (Example 2) in 60 ml of toluene. The emulsion produced is warmed at 97° (reflux). After 1 h, the emulsion is cooled to room temperature and diluted with 20 ml of water. The two phases are separated, and the organic phase is dried over MgSO4 and evaporated in vacuo. The liquid crude product is purified by medium-pressure chromatography. 3.1 g of N-butyl-N-acetyl-2,4-difluoroaniline are obtained as a brownish oil.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05026625
Quelldatensatzuspto-grants-1991_06
ORD IDord-97ddca6efec049b8af0e4bcb966496bc
Quellennotizuspto-grants-1991_06