Reaktionsgleichung
[Cl:1][C:2]1[C:10]([Cl:11])=[C:9]([CH3:12])[CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].S(Cl)([Cl:15])=O>C1(C)C=CC=CC=1>[Cl:1][C:2]1[C:10]([Cl:11])=[C:9]([CH3:12])[CH:8]=[CH:7][C:3]=1[C:4]([Cl:15])=[O:5]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2,3-Dichloro-4-methylbenzoic acid (I70) (5.90 g, 26.2 mmol) and thionyl chloride (30 mL, 411 mmol) were heated at 85° C. for 4 hr in toluene (100 mL). The solvents were removed in vacuo and the residue was azeotroped with toluene (3×100 mL). The residue was used in subsequent steps without further purification assuming 100% yield. Compound not characterised at this step.
Aufarbeitung
- customThe solvents were removed in vacuo
- customthe residue was azeotroped with toluene (3×100 mL)
- customThe residue was used in subsequent steps without further purification
Quellen und Nachweise
- ORD-Eintrag
- ord-0b4f10b90a43412d8a4e0eb289a0de2d
- Quelldatensatz
- uspto-grants-2013_08
- Patentnummer
- US08501946B2
Verknüpfte Notizen
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