Hydrochloric Acid → 3-(Pent-2-en-3-yl)-2,2'-bitiophene
Reaktionsgleichung
[S:1]1[CH:5]=[CH:4][C:3]([C:6](O)([CH2:9][CH3:10])[CH2:7][CH3:8])=[C:2]1[C:12]1[S:13][CH:14]=[CH:15][CH:16]=1.Cl>C(O)(=O)C>[CH3:8][CH:7]=[C:6]([C:3]1[CH:4]=[CH:5][S:1][C:2]=1[C:12]1[S:13][CH:14]=[CH:15][CH:16]=1)[CH2:9][CH3:10]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
3-(2,2′-bithiophene-3-yl)pentan-3-ol (IIa) (0.100 g, 0.40 mmol) was dissolved in acetic acid (69 mL). A solution of concentrated HCl (0.28 mL) in acetic acid (15 mL) was added via syringe to the reaction mixture. The solution was refluxed for 4 h followed by an extraction with chloroform, washing and drying over MgSO4. The solvent was removed in vacuo. The residue was purified by column chromatography on silica (n-Hexane). (0.070 g, 75%).
Aufarbeitung
- temperatureThe solution was refluxed for 4 h
- extractionfollowed by an extraction with chloroform
- washwashing
- dry with materialdrying over MgSO4
- customThe solvent was removed in vacuo
- customThe residue was purified by column chromatography on silica (n-Hexane)
Quellen und Nachweise
- ORD-Eintrag
- ord-c408fb10b8f3415da4b6d5c154bfe0f1
- Quelldatensatz
- uspto-grants-2012_12
- Patentnummer
- US08329923B2
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