Reaktionsgleichung
[CH3:1][C:2]1[O:3][C:4]([CH3:11])=[C:5]([CH3:10])[C:6]=1[C:7](O)=[O:8].S(Cl)([Cl:14])=O>C1(C)C=CC=CC=1>[CH3:1][C:2]1[O:3][C:4]([CH3:11])=[C:5]([CH3:10])[C:6]=1[C:7]([Cl:14])=[O:8]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
2,4,5-Trimethyl-3-furancarbonyl chloride was prepared by refluxing 2,4,5-trimethyl-3-furancarboxylic acid (20.0 g) with thionyl chloride (20 ml) in toluene (75 ml) for 3 hours. The toluene and excess thionyl chloride were removed on a rotary evaporator and the residue distilled (b.p. 95°-97° C. at ca. 12 mm).
Aufarbeitung
- customThe toluene and excess thionyl chloride were removed on a rotary evaporator
- distillationthe residue distilled (b.p. 95°-97° C. at ca. 12 mm)
Quellen und Nachweise
- ORD-Eintrag
- ord-6e3063683a874e328e6fedbea747620b
- Quelldatensatz
- uspto-grants-1993_12
- Patentnummer
- US05268389
Verknüpfte Notizen
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