Hydrochloric Acid → 5-(3,4-Dimethoxyphenyl)pentanoic acid
Reaktionsgleichung
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([C:11](=O)[CH2:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].Cl>[Zn].Cl[Hg]Cl>[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH2:11][CH2:12][CH2:13][CH2:14][C:15]([OH:17])=[O:16])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10]Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture containing 37.6 g of the product obtained in Example 38 and 64 g of zinc turnings (treated with a solution of HgCl2), 55 ml of tolueneand 220 ml of cone. hydrochloric acid was refluxed for 1 h. Toluene phase was separated and evaporated in vacuo. The residue was crystallized from toluene-petroleum ether, yield 11.5 g (32%).
Aufarbeitung
- customToluene phase was separated
- customevaporated in vacuo
- customThe residue was crystallized from toluene-petroleum ether, yield 11.5 g (32%)
Quellen und Nachweise
- ORD-Eintrag
- ord-6dd749b1dbef45b0a87a1fc4a2d2fe04
- Quelldatensatz
- uspto-grants-1995_08
- Patentnummer
- US05446194
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