Reaktionsgleichung
[CH2:1](Cl)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C([S:16][C:17]1[S:18][CH2:19][CH2:20][N:21]=1)C1C=CC=CC=1>CO>[CH2:1]([N:21]1[CH:20]=[CH:19][S:18][C:17]1=[S:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 150 °C
Versuchsvorschrift
12.7 g (0.1 mole) of benzylchloride were added to 209.2 g (1 mole) of 2-benzylthio-thiazoline and the mixture was heated to 150° C. for eight hours. The mixture was allowed to cool down to 70° C. and 500 ml of methanol were added. The reaction mixture was allowed to cool down to room temperature and stirred for an additional hour; N-benzyl-thiazoline-thion precipitated from the medium as a white crystalline product, was isolated by filtration and washed twice with 10 ml of methanol. The crude product was recrystallized from a minimum of acetonitrile. 146 g of N-benzyl-thiazolinethion were isolated and sulfonated as described below.
Aufarbeitung
- temperatureto cool down to 70° C.
- temperatureto cool down to room temperature
- customN-benzyl-thiazoline-thion precipitated from the medium as a white crystalline product
- customwas isolated by filtration
- washwashed twice with 10 ml of methanol
- customThe crude product was recrystallized from a minimum of acetonitrile
Quellen und Nachweise
- ORD-Eintrag
- ord-789ad516cc7a459dbf3e7dacc4f95292
- Quelldatensatz
- uspto-grants-2004_05
- Patentnummer
- US06733947B2
Verknüpfte Notizen
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