Hydrochloric Acid → Isoquinoline, 6-hydroxy-1,2,3,4-tetrahydro-, hydrochloride
Reaktionsgleichung
[ClH:1].[OH:2][C:3]1[CH:4]=[C:5]([CH:9]=[CH:10][CH:11]=1)[CH2:6][CH2:7][NH2:8].Cl.[CH3:13]O>C=O>[ClH:1].[CH2:13]1[C:9]2[C:5](=[CH:4][C:3]([OH:2])=[CH:11][CH:10]=2)[CH2:6][CH2:7][NH:8]1Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 45 °C
Versuchsvorschrift
To a solution of 3-hydroxyphenethylamine hydrochloride (3.0 g) in methanol (6 mL), formaldehyde (37% aqueous solution, 2.7 mL) and a catalytic amount of concentrated hydrochloric acid were added, followed by stirring at 45° C. for 18 hours. The reaction mixture was concentrated and the obtained solid was washed with a mixed solvent of diisopropyl ether-methanol (1:2) to thereby give the title compound (2.8 g) having the following physical properties.
Aufarbeitung
- concentrationThe reaction mixture was concentrated
- washthe obtained solid was washed with a mixed solvent of diisopropyl ether-methanol (1:2)
Quellen und Nachweise
- ORD-Eintrag
- ord-a1a2dd69e7f24574a455943c9c51ee2a
- Quelldatensatz
- uspto-grants-2011_10
- Patentnummer
- US08039674B2
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