Reaktion #49959
ord-de9bab9b5e424189ac8c17363b982488
Reaktionsgleichung
o-anisidine
benzoyl isothiocyanate
→
N-(o-methoxyphenyl)thiourea
Ausbeute 57.1%
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Temperaturunder reflux for 2 hours
- 2FiltrationThe resulting crystals were collected by filtration
- 3Waschenwashed with cold acetone
- 4Sonstigedried under reduced pressure
- 5workup.ADDITIONThe crystals were added to 50 ml of 30% methylamine-methanol
- 6workup.STIRRINGthe mixture was stirred at room temperature overnight
- 7EinengenThe reaction mixture was concentrated to dryness under reduced pressure
- 8Waschenthe residue was washed with ethanol-ethyl acetate
- 9Sonstigedried under reduced pressure
Vorschrift
To 50 ml of acetone were added 2.46 g of o-anisidine and 3.75 g of benzoyl isothiocyanate, and the mixture is stirred under reflux for 2 hours and, then, allowed to stand overnight in a refrigerator at 5° C. The resulting crystals were collected by filtration, washed with cold acetone and dried under reduced pressure. The crystals were added to 50 ml of 30% methylamine-methanol and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated to dryness under reduced pressure, and the residue was washed with ethanol-ethyl acetate and dried under reduced pressure. The procedure provided 2.08 g of N-(o-methoxyphenyl)thiourea.