Pyridine → 2-chloro-N-(3-chloro-4-fluorophenyl)acetamide

To 130 ml of toluene was added, with stirring, 24.0 g (0.165 mole) of 3-chloro-4-fluoroaniline and 13.5 ml (0.166 mole) of pyridine. The resulting solution was cooled to ca 0° C. and 13.2 ml (0.166 mole) of 2-chloroacetyl chloride was added. The reaction mixture was stirred at room temperature for 5 hours and then it was extracted twice with 100 ml of lN hydrochloric acid, followed by 100 ml of saturated sodium chloride solution. The resulting toluene solution was dried using magnesium sulfate, and then it was concentrated in vacuo to give 32.6 g (88% yield) of N-(2-chloroacetyl)-3-chloro-4-fluoroaniline.

1. temperatureThe resulting solution was cooled to ca 0° C.
2. stirringThe reaction mixture was stirred at room temperature for 5 hours
3. extractionit was extracted twice with 100 ml of lN hydrochloric acid
4. dry with materialThe resulting toluene solution was dried
5. concentrationit was concentrated in vacuo

ORD-Eintrag

ord-09e10b9cb40049dabfbb21aac122792a

Quelldatensatz

uspto-grants-1987_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US04658037