Thionyl Chloride → Benzhydrylthioacetyl chloride
Reaktionsgleichung
[CH:1]([CH2:14][C:15](O)=[S:16])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.S(Cl)([Cl:20])=O>C1C=CC=CC=1>[CH:1]([CH2:14][C:15]([Cl:20])=[S:16])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
19.5 g (0.076 mol) of benzhydrylthioacetic acid in 114 ml of benzene are placed in a three-necked flask provided with a condenser and a dropping funnel. The mixture is heated and 19 ml of thionyl chloride are added drop by drop. Once the addition is complete, the reflux is continued for about 1 hour, cooling and filtering are carried out and the benzene and the excess thionyl chloride and then evaporated. In this way, a clear orange oil is obtained.
Aufarbeitung
- customprovided with a condenser and a dropping funnel
- temperatureThe mixture is heated
- additionOnce the addition
- temperaturecooling
- filtrationfiltering
- customthe benzene and the excess thionyl chloride and then evaporated
- customIn this way, a clear orange oil is obtained
Quellen und Nachweise
- ORD-Eintrag
- ord-2abe3ad6ca93492494aa196319ebb94c
- Quelldatensatz
- uspto-grants-1979_12
- Patentnummer
- US04177290
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