Thionyl Chloride → 3-Methyl-6-(phenylthio)-benzyl chloride
Reaktionsgleichung
[CH3:1][C:2]1[CH:3]=[C:4]([C:7]([S:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:8][CH:9]=1)[CH2:5]O.S(Cl)([Cl:19])=O>C1C=CC=CC=1>[CH3:1][C:2]1[CH:3]=[C:4]([C:7]([S:10][C:11]2[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=2)=[CH:8][CH:9]=1)[CH2:5][Cl:19]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
570.7 g of 3-methyl-6-(phenylthio)-benzyl alcohol are dissolved in 1.5 litres of benzene and heated under reflux. There are added dropwise thereto within 45 minutes 352 ml of thionyl chloride and the mixture is boiled for a further 90 minutes. Then the mixture is concentrated under reduced pressure and there is obtained 3-methyl-6-(phenylthio)-benzyl chloride as a red-brown oil.
Aufarbeitung
- temperatureheated
- temperatureunder reflux
- additionThere are added dropwise
- concentrationThen the mixture is concentrated under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-5c9ac29b07614bd8afa424a4ace031fa
- Quelldatensatz
- uspto-grants-1977_02
- Patentnummer
- US04006144
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