Thionyl Chloride → 2-Methyl-2-(4-pyridinylthio)propanoyl chloride
Reaktionsgleichung
[CH3:1][C:2]([S:7][C:8]1[CH:13]=[CH:12][N:11]=[CH:10][CH:9]=1)([CH3:6])[C:3](O)=[O:4].S(Cl)([Cl:16])=O>>[CH3:1][C:2]([S:7][C:8]1[CH:13]=[CH:12][N:11]=[CH:10][CH:9]=1)([CH3:6])[C:3]([Cl:16])=[O:4]Komponenten
3
Versuchsvorschrift
9.7 g of the product from step (b) was refluxed for 2 1/2 hours in 225 ml thionyl chloride. The mixture was concentrated in vacuo. The residue was triturated and concentrated in vacuo two times with toluene to yield a white solid which showed the expected carbonyl shift in the IR, indicative of an acid chloride.
Aufarbeitung
- concentrationThe mixture was concentrated in vacuo
- customThe residue was triturated
- concentrationconcentrated in vacuo two times with toluene
- customto yield a white solid which
Quellen und Nachweise
- ORD-Eintrag
- ord-5985fda140f3428596db54047ef9ad24
- Quelldatensatz
- uspto-grants-1989_09
- Patentnummer
- US04866068
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