Reaktionsgleichung
[ClH:1].[CH3:2][C:3]([NH:6][CH2:7][C@H:8]([OH:22])[CH2:9][O:10][C:11]1[C:12]([N:16]2[CH2:21][CH2:20][O:19][CH2:18][CH2:17]2)=[N:13][S:14][N:15]=1)([CH3:5])[CH3:4]>C(O)(C)C>[ClH:1].[CH3:5][C:3]([NH:6][CH2:7][C@H:8]([OH:22])[CH2:9][O:10][C:11]1[C:12]([N:16]2[CH2:21][CH2:20][O:19][CH2:18][CH2:17]2)=[N:13][S:14][N:15]=1)([CH3:2])[CH3:4]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
0.8 ml of a 7M HCl solution in isopropanol was added dropwise to a magnetically stirred solution of timolol (1.4 g) in isopropanol (30 ml). The solution was stirred for 30 minutes. The reaction mixture was freed of the solvent at reduced pressure. 1.47 g of pure product was obtained (yield 91%).
Quellen und Nachweise
- ORD-Eintrag
- ord-4441b34afb6240a7bee27d9b58d30fb9
- Quelldatensatz
- uspto-grants-2001_06
- Patentnummer
- US06242432B1
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