Thionyl Chloride → HCID 20338242, Verbindung
Reaktionsgleichung
[CH2:1]([N:8]([CH2:18][CH2:19]O)[C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O=S(Cl)[Cl:23]>>[ClH:23].[CH2:1]([N:8]([CH2:18][CH2:19][Cl:23])[C:9]1[CH:17]=[CH:16][CH:15]=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
3
Versuchsvorschrift
2-[Benzyl(2-hydroxyethyl)amino]benzamide (10 g) was added at 0° to 50 ml SOCl2, stirred 71/2 hours at room temperature and left overnight. The mixture was concentrated on the rotovap, ethyl acetate added and the solid filtered to give 11 g product, m.171-4°.
Aufarbeitung
- waitleft overnight
- concentrationThe mixture was concentrated on the rotovap, ethyl acetate
- additionadded
- filtrationthe solid filtered
Quellen und Nachweise
- ORD-Eintrag
- ord-bb6450f9ed414956a3d41b5dfc4f6bdd
- Quelldatensatz
- uspto-grants-1977_11
- Patentnummer
- US04060526
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