Reaktionsgleichung
[C:1]1([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7](O)([CH:9]=[C:10]=[CH2:11])[CH3:8].Cl.C[OH:21]>>[C:1]1([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[CH:6]=[CH:5][CH:4]=[CH:3][C:2]=1[C:7](=[CH:9][C:10](=[O:21])[CH3:11])[CH3:8]Komponenten
4
Versuchsvorschrift
To a solution of 10 g. of 2-(p-biphenylyl)-3,4-pentadien-2-ol in 200 ml. of anhydrous methanol is added 3 ml. of concentrated hydrochloric acid (12 N). The resulting mixture is stirred at room temperaure for 3 hours and then in an ice bath for 2 hours. Solids formed are filtered off and recrystallized from pentane to obtain 2-(p-biphenylyl)-2-penten-4-one, m.p. 130°-133° C. 2-(p-(biphenylyl)-4-chloro-2,4-pentadiene, byproduct, remains in the mother liquor.
Aufarbeitung
- waitin an ice bath for 2 hours
- customSolids formed
- filtrationare filtered off
- customrecrystallized from pentane
Quellen und Nachweise
- ORD-Eintrag
- ord-ff9d386997e44cd282bcd919d45b9317
- Quelldatensatz
- uspto-grants-1982_08
- Patentnummer
- US04344966
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