Reaktionsgleichung
[C:1]1([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][CH:8]([CH2:12][CH3:13])[C:9](O)=[O:10].S(Cl)([Cl:22])=O>>[C:1]1([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[CH2:7][CH:8]([CH2:12][CH3:13])[C:9]([Cl:22])=[O:10]Komponenten
3
Versuchsvorschrift
To a 300-ml three-necked round flask (equipped with a stirrer tip, a Zimroth condenser, a thermometer and a NaOH trap) were fed 39.9 g (157.2 mmol) of 3-(2-biphenylyl)-2-ethylpropionic acid and 77.7 ml (1,065 mmol) of thionyl chloride, and the contents in the flask were refluxed for 2.5 hours in a nitrogen atmosphere. After the reaction was completed, the unreacted thionyl chloride was distilled off under reduced pressure to obtain 45.6 g of a coarse product of an yellow-orange liquid. This acid chloride was used for the next reaction without any further purification.
Aufarbeitung
- customTo a 300-ml three-necked round flask (equipped with a stirrer tip
- temperaturethe contents in the flask were refluxed for 2.5 hours in a nitrogen atmosphere
- distillationthe unreacted thionyl chloride was distilled off under reduced pressure
Quellen und Nachweise
- ORD-Eintrag
- ord-22a828ed0c9149a6841496306782a51a
- Quelldatensatz
- uspto-grants-2000_12
- Patentnummer
- US06156844
Verknüpfte Notizen
Wird geladen…