Reaktion #607460
ord-4c663eee69d540ffb2f679782993721e
Reaktionsgleichung
thionyl chloride
3-(2-hydroxyethyl)quinazoline-4 (3H)-one
→
3-(2-chloroethyl) quinazoline-4 (3H)-one
Ausbeute 82.0%
Reagenzien
Keine
Lösungsmittel
Reaktionsbedingungen
Temperatur
85°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.
Aufarbeitung
- 1Sonstigeforming a white suspension
- 2workup.WAITThe reaction medium was kept at this temperature under agitation for thirty minutes
- 3workup.WAITafter which it was left
- 4Temperaturto cool to about 40° C
- 5Sonstigeforming a pinkish suspension, which
- 6Filtrationvacuum filtered
- 7Waschenwashed with three portions of 10 mL of an ethanol/water mixture (50% v/v)
Vorschrift
This thionyl chloride (1,095 mL, 15 mmol) was added to 3-(2-hydroxyethyl)quinazoline-4 (3H)-one (2.0 g, 10.52 mmol) in a reactor, forming a white suspension that heated spontaneously to 85° C. The reaction medium was kept at this temperature under agitation for thirty minutes, after which it was left to cool to about 40° C. Next, 50 mL of water was added, forming a pinkish suspension, which was kept under agitation for two hours. The product was then vacuum filtered and washed with three portions of 10 mL of an ethanol/water mixture (50% v/v), yielding 3-(2-chloroethyl) quinazoline-4 (3H)-one as a pale white solid (1.8 g, 8.63 mmol, yield=82%).