Formaldehyde → 2-(Pyrimidin-4-yl)ethanol
Reaktionsgleichung
[CH3:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][N:3]=1.[CH2:8]=[O:9]>CCOCC>[OH:9][CH2:8][CH2:1][C:2]1[CH:7]=[CH:6][N:5]=[CH:4][N:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 4-methylpyrimidine (10 g, 106 mmol) and para-formaldehyde (3 g) was stirred in a 50 mL sealed capacity pressure vessel at 165° C. for 3.5 hours. After cooling, ether was added and the solvents evaporated to afford an oil. This was purified by silica column chromatography using a Flashmaster system, eluting with dichloromethane, then chloroform, ether, and finally ethyl acetate. The ethyl acetate fractions were evaporated to afford the title compound as an oil.
Aufarbeitung
- customsealed capacity pressure vessel at 165° C. for 3.5 hours
- temperatureAfter cooling
- customthe solvents evaporated
- customto afford an oil
- customThis was purified by silica column chromatography
- washeluting with dichloromethane
- customThe ethyl acetate fractions were evaporated
Quellen und Nachweise
- ORD-Eintrag
- ord-24aa06d178004867a09c8cf2f8c473d2
- Quelldatensatz
- uspto-grants-2007_08
- Patentnummer
- US07259163B2
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