Dimethyl 4-hydroxyisophthalate → 2-Hydroxy-5-(methoxycarbonyl)benzoic acid
Reaktionsgleichung
[CH3:1][O:2][C:3](=[O:15])[C:4]1[CH:13]=[CH:12][C:11]([OH:14])=[C:6]([C:7]([O:9]C)=[O:8])[CH:5]=1>N1C=CC=CC=1>[OH:14][C:11]1[CH:12]=[CH:13][C:4]([C:3]([O:2][CH3:1])=[O:15])=[CH:5][C:6]=1[C:7]([OH:9])=[O:8]Komponenten
3
Edukt 1
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A solution of dimethyl-4-hydroxyisophthalate (10.0 g, 47.6 mmol) in pyridine (70 mL) was heated to reflux for 15 h. The reaction mixture was concentrated in vacuo and acidified with 1N HCl at 0° C. The resulting solid was collected by filtration, washed with water and dried in vacuo to provide the title compound (9.3 g, 100%) as a white solid. 1H NMR (DMSO-d6) δ 8.40 (d, J=2.0 Hz, 1H), 8.06 (dd, J=8.4, 2.0 Hz, 1H), 7.07 (d, J=8.4 Hz, 1H), 3.84 (s, 3H); MS(ESI−) m/z 195.2 (M−H)−.
Aufarbeitung
- temperatureto reflux for 15 h
- concentrationThe reaction mixture was concentrated in vacuo
- customacidified with 1N HCl at 0° C
- filtrationThe resulting solid was collected by filtration
- washwashed with water
- customdried in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-7145ff93439d4f829dde23737dfd7ee9
- Quelldatensatz
- uspto-grants-2016_05
- Patentnummer
- US09346795B2
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