Sodium Hydroxide → 4-(2,3-Pentadienyloxy)benzenesulfonic acid sodium salt
Reaktionsgleichung
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([O-:11])(=[O:10])=[O:9])=[CH:4][CH:3]=1.[Na+:12].[OH-].[Na+]>C(O)(C)C>[Na+:12].[CH2:4]([O:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([O-:11])(=[O:9])=[O:10])=[CH:4][CH:3]=1)[CH:3]=[C:2]=[CH:7][CH3:6]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 67.5 °C
Versuchsvorschrift
To a suspension of sodium 4-hydroxybenzenesulfonate (1.3 g, 5.6 mmol) in iso-propanol (20 ml) was added product from Example 8 (700 mg, 6.8 mmol) followed by 1N sodium hydroxide (6.1 ml, 6.1 mmol) and the resulting mixture was heated at 65-70° C. for 15 hours. The reaction mixture was concentrated in vacuo, the solid collected and washed with diethy ether to give 880 mg (53%) of the product as a solid.
Aufarbeitung
- concentrationThe reaction mixture was concentrated in vacuo
- customthe solid collected
- washwashed with diethy ether
Quellen und Nachweise
- ORD-Eintrag
- ord-4692e8bac9244e86b71ae4742b49000c
- Quelldatensatz
- uspto-grants-2007_10
- Patentnummer
- US07282496B2
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