Reaktionsgleichung
[I:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9]Br.ClC1C=CC(C2C=CC=CC=2)=CC=1.C(OCCCC1C=CC=CC=1)(=O)CC([O-])=[O:27]>>[I:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1[CH2:8][CH2:9][OH:27]Komponenten
4
Versuchsvorschrift
The title compound was synthesized by a sequence similar to that for Example 87 except that 2-(2-iodophenyl)ethyl bromide and commercially available diethyl phenethyl malonate were used in lieu of the 4-chlorobiphenyl and phenylpropyl malonate respectively. The final product was recrystallized from chloroform to give a fluffy, white solid (mp: melts/softens over a broad range starting at 50° C.; the bulk of the sample melts at 189°-190° C.).
Aufarbeitung
- customThe final product was recrystallized from chloroform
- customto give a fluffy, white solid (mp
- customstarting at 50° C.
Quellen und Nachweise
- ORD-Eintrag
- ord-85fe9cb35a9243cfaf8edd9d1c8b6108
- Quelldatensatz
- uspto-grants-1999_03
- Patentnummer
- US05886024
Verknüpfte Notizen
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