Thionyl Chloride → 4-(Chloromethyl)-2-cyclopropylthiazole hydrochloride
Reaktionsgleichung
[CH:1]1([C:4]2[S:5][CH:6]=[C:7]([CH2:9]O)[N:8]=2)[CH2:3][CH2:2]1.S(Cl)([Cl:13])=O>C(Cl)(Cl)Cl>[ClH:13].[CH:1]1([C:4]2[S:5][CH:6]=[C:7]([CH2:9][Cl:13])[N:8]=2)[CH2:3][CH2:2]1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
In chloroform (10 ml) was dissolved 2-cyclopropyl-4-hydroxymethylthiazole (0.9 g), to which was added dropwise, under ice-cooling, thionyl chloride (0.68 ml), followed by stirring for 30 minutes at room temperature. Excess thionyl chloride was distilled off under reduced pressure. To the residue was added diethyl ether to yield 2-cyclopropyl-4-chloromethyl thiazole hydrochloride (1.1 g) as pale brown powder. m.p. 108°-110° C.
Aufarbeitung
- additionto which was added dropwise, under ice-
- temperaturecooling
- distillationExcess thionyl chloride was distilled off under reduced pressure
- additionTo the residue was added diethyl ether
Quellen und Nachweise
- ORD-Eintrag
- ord-21dbd786b3184c6bb3ae790f12765813
- Quelldatensatz
- uspto-grants-1995_04
- Patentnummer
- US05405861
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