Thionyl Chloride → N-((4-(chloromethyl)phenyl)methyl)acetamide
Reaktionsgleichung
O[CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][NH:10][C:11](=[O:13])[CH3:12])=[CH:5][CH:4]=1.S(Cl)([Cl:16])=O>C(Cl)(Cl)Cl>[Cl:16][CH2:2][C:3]1[CH:8]=[CH:7][C:6]([CH2:9][NH:10][C:11](=[O:13])[CH3:12])=[CH:5][CH:4]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
To a solution of N-(4-hydroxymethylphenylmethyl)acetamide (1.5 g) in chloroform (50 ml) was added thionyl chloride (0.73 ml) and the mixture was refluxed under heating for 1 hr. The solvent was evaporated and the obtained residue was crystallized from ethyl acetate to give the title compound (1.8 g) as pale-yellow crystals.
Aufarbeitung
- temperaturethe mixture was refluxed
- temperatureunder heating for 1 hr
- customThe solvent was evaporated
- customthe obtained residue was crystallized from ethyl acetate
Quellen und Nachweise
- ORD-Eintrag
- ord-0c7d81dfc33e4dad9e5e8384eff8668c
- Quelldatensatz
- uspto-grants-2002_09
- Patentnummer
- US06455528B1
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