Styrene → HCID 18348271, compound
Reaction equation
[F:1][C:2]1[CH:7]=[C:6]([CH2:8][CH2:9][C:10]2[CH:15]=[CH:14][C:13]([O:16][CH2:17][CH3:18])=[CH:12][CH:11]=2)[CH:5]=[C:4]([F:19])[C:3]=1OB(O)O.FC1C=C(C=C(F)C=1)C=O.[I-].C(OC1C=CC(C[P+](C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1)C.C=CC1C=CC=CC=1.Br[C:73]1[CH:78]=[CH:77][C:76]([CH2:79][CH2:80][CH3:81])=[CH:75][CH:74]=1.C([O-])([O-])=O.[Na+].[Na+]>C1(C)C=CC=CC=1>[CH2:17]([O:16][C:13]1[CH:14]=[CH:15][C:10]([CH2:9][CH2:8][C:6]2[CH:7]=[C:2]([F:1])[C:3]([C:73]3[CH:78]=[CH:77][C:76]([CH2:79][CH2:80][CH3:81])=[CH:75][CH:74]=3)=[C:4]([F:19])[CH:5]=2)=[CH:11][CH:12]=1)[CH3:18]Participants
8
Procedure
A mixture of 9.2 g of 2,6-difluoro-4-[2-(p-ethoxyphenyl)ethyl]phenylboric acid (prepared by reacting 3,5-difluorobenzaldehyde with p-ethoxybenzyltriphenylphosphonium iodide by the Wittig method and subsequently hydrogenating the resulting styrene derivative on Pd/C), 6.0 g of 1-bromo-4-n-propylbenzene, 38 ml of 2 ml [sic] aqueous Na2CO3 solution, 0.6 g of tetrakis(triphenyl-phosphine)palladium(0) an d 75 ml of toluene is refluxed for two hours. The aqueous phase is extracted twice with toluene and combined with the organic phase. Conventional aqueous work-up and chromatographic purification of the residue give 4-[2-(p-ethoxyphenyl)ethyl]-2,6-difluoro-4′-n-propylbiphenyl.
Workup
- customprepared
- temperatureis refluxed for two hours
- extractionThe aqueous phase is extracted twice with toluene
- customConventional aqueous work-up and chromatographic purification of the residue
Sources & evidence
- ORD record
- ord-79d87b806a0647c2bdbdcb58288d9bd7
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06326066B1
Reaction notes
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