Hydrochloric Acid → HCID 12824088, Verbindung
Reaktionsgleichung
[CH3:1][O:2][C:3]1[C:4](=[O:19])[C:5]([CH2:13][CH2:14][CH2:15][C:16]([OH:18])=[O:17])=[C:6]([CH3:12])[C:7](=[O:11])[C:8]=1[O:9][CH3:10].Cl.[CH2:21](O)[CH3:22]>>[CH3:1][O:2][C:3]1[C:4](=[O:19])[C:5]([CH2:13][CH2:14][CH2:15][C:16]([O:18][CH2:21][CH3:22])=[O:17])=[C:6]([CH3:12])[C:7](=[O:11])[C:8]=1[O:9][CH3:10]Komponenten
4
Versuchsvorschrift
A solution of 2,3-dimethoxy-5-methyl-6-(3'-carboxypropyl)-1,4-benzoquinone (formula I-2 wherein R=H3CO, n=2 in the free form) (0.8 part) in ethanol (3 volume parts) saturated with dry hydrogen chloride was stirred at room temperature for 1 hour. The residue upon removal of the solvent was subjected to chromatography on silica gel and eluted with chloroform to give 2,3-dimethoxy-5-methyl-6-(3'-ethoxycarbonylpropyl)-1,4-benzoquinone (formula I-2 wherein R=H3CO, n=2, in the form of ethyl ester) (0.88 part) as an orange oil.
Aufarbeitung
- customThe residue upon removal of the solvent
- washeluted with chloroform
Quellen und Nachweise
- ORD-Eintrag
- ord-fca4c7de4faa452b892a794b7f7516de
- Quelldatensatz
- uspto-grants-1981_06
- Patentnummer
- US04271083
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