Hydrochloric Acid → Ethyl 7-hydroxychromane-2-carboxylate
Reaktionsgleichung
[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6](=O)[CH:7]=[C:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[O:9]2)=[CH:4][CH:3]=1.Cl>[Pd].CCO>[OH:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH:8]([C:12]([O:14][CH2:15][CH3:16])=[O:13])[O:9]2)=[CH:4][CH:3]=1Komponenten
5
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
To a large hydrogenation vessel were added ethyl 7-hydroxychromone-2-carboxylate (=ethyl 7-hydroxy-4-oxo-4H-chromene-2-carboxylate) (675.4 g, 2.88 mol), EtOH 4 liters, conc. hydrochloric acid 40 ml. The resulting suspension was combined with 5% Pd/C 68 g, and subjected to hydrogenation condition (H2, 40 psi, rt) overnight. The reaction mixture was filtered through a pad of celite to remove the catalyst. The filtrate was concentrated to give thick oily material, which solidified upon standing. Tan solid 630.1 g (98%).
Aufarbeitung
- customsubjected to hydrogenation condition (H2, 40 psi, rt) overnight
- filtrationThe reaction mixture was filtered through a pad of celite
- customto remove the catalyst
- concentrationThe filtrate was concentrated
- customto give thick oily material, which
Quellen und Nachweise
- ORD-Eintrag
- ord-4b45c41df47340bbac4c6a7fe9c76a07
- Quelldatensatz
- uspto-grants-2004_03
- Patentnummer
- US06713508B2
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