Acetic Anhydride → 1H,3H-Thieno[3,4-c]furan-1,3-dione
Reaktionsgleichung
[S:1]1[CH:5]=[C:4]([C:6]([OH:8])=O)[C:3]([C:9]([OH:11])=[O:10])=[CH:2]1.C(OC(=O)C)(=O)C>>[C:6]1(=[O:8])[C:4]2=[CH:5][S:1][CH:2]=[C:3]2[C:9](=[O:10])[O:11]1Komponenten
3
Versuchsvorschrift
In a 250 mL single-neck round-bottom flask equipped with reflux condenser, 3,4-thiophenedicarboxylic acid (Frontier Scientific, 4.000 g, 0.02325 mol) was heated to 120° C. with acetic anhydride for 6 hours. The reaction was then cooled to room temperature and the solvent was removed under reduced pressure to yield a dark brown solid. The crude product was recrystallized from toluene to yield pale yellow needles in quantitative yield.
Aufarbeitung
- customIn a 250 mL single-neck round-bottom flask equipped
- temperaturewith reflux condenser
- customthe solvent was removed under reduced pressure
- customto yield a dark brown solid
- customThe crude product was recrystallized from toluene
- customto yield pale yellow needles in quantitative yield
Quellen und Nachweise
- ORD-Eintrag
- ord-0c388784e8e84e07bbfc2cc9cb2978ed
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09355787B2
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