Benzyl Chloride → Benzyl thioacetimidate hydrochloride
Reaktionsgleichung
[C:1]([NH2:4])(=[S:3])[CH3:2].[CH2:5]([Cl:12])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1>C(Cl)(Cl)Cl>[ClH:12].[CH2:5]([S:3][C:1](=[NH:4])[CH3:2])[C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of thioacetamide (15.0 g, 0.20 mol) and benzyl chloride (25.3 g, 0.20 mol) in chloroform (75 ml) was heated under reflux for 90 minutes (the thioacetamide required ˜40 minutes to go into solution). The reaction mixture was then allowed to cool to room temperature and was then stood at 0° C. overnight, when colourless crystals formed as a layer on the surface. The product was filtered off, washed with cold 10% ether-chloroform and sucked dry to give the title compound (25.55 g) as colourless prisms. Mpt.=161°-163° C.
Aufarbeitung
- temperaturewas heated
- customwhen colourless crystals formed as a layer on the surface
- filtrationThe product was filtered off
- washwashed with cold 10% ether-chloroform
- customsucked dry
Quellen und Nachweise
- ORD-Eintrag
- ord-84278d0b88bd47148b38faca86770b5f
- Quelldatensatz
- uspto-grants-2007_04
- Patentnummer
- USRE039576E1
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