Acetic Anhydride → 2-Acetamido-4-fluorotoluene
Reaktionsgleichung
C(O[C:5](=[O:7])[CH3:6])(=O)C.[NH2:8][C:9]1[CH:14]=[C:13]([F:15])[CH:12]=[CH:11][C:10]=1[CH3:16]>O>[C:5]([NH:8][C:9]1[CH:14]=[C:13]([F:15])[CH:12]=[CH:11][C:10]=1[CH3:16])(=[O:7])[CH3:6]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
139 ml (150.4 g; 1.473 molecules) of acetic anhydride were added in one portion to a hot (35° ) stirred mixture of 90.0 g (0.719 molecule) of 2-amino-4-fluorotoluene (1) in 513 ml of water. The temperature rose to 73° and a solid separated out (by precipitation). The mixture was cooled to ambient temperature and the solid was recovered on a filter, washed with water (525 ml), then dried in vacuo at 80°, yield: 115.7 g (96.2%); m.p.: 127°-128°. The material was still transformable.
Aufarbeitung
- customrose to 73°
- customa solid separated out (by precipitation)
- customthe solid was recovered on a filter
- washwashed with water (525 ml)
- customdried in vacuo at 80°
Quellen und Nachweise
- ORD-Eintrag
- ord-2df4915d69f94b4eba49365d1c73085f
- Quelldatensatz
- uspto-grants-1982_01
- Patentnummer
- US04312862
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