Reaktionsgleichung
[CH3:1][O:2][C:3](=[O:15])[CH:4]=[C:5]1[CH2:14][CH2:13][C:8]2([O:12][CH2:11][CH2:10][O:9]2)[CH2:7][CH2:6]1.[H][H]>[C].[Pd].C(O)C>[CH3:1][O:2][C:3](=[O:15])[CH2:4][CH:5]1[CH2:14][CH2:13][C:8]2([O:9][CH2:10][CH2:11][O:12]2)[CH2:7][CH2:6]1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
An ethanol (50 mL) suspension of (1,4-dioxa-spiro[4.5]dec-8-ylidene)-acetic acid methyl ester (6.57 g) obtained in Example (1a) and palladium carbon (10% by weight) was hydrogen-reduced at room temperature for 24 hours. The reaction mixture was filtered and concentrated. The residue was purified by chromatography (hexane/ethyl acetate=5:1) to obtain the title compound (4.99 g, 75%) as a colorless oil.
Aufarbeitung
- filtrationThe reaction mixture was filtered
- concentrationconcentrated
- customThe residue was purified by chromatography (hexane/ethyl acetate=5:1)
Quellen und Nachweise
- ORD-Eintrag
- ord-b79eea263fae4da280a7ec3f90fa45f7
- Quelldatensatz
- uspto-grants-2014_05
- Patentnummer
- US08735425B2
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