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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2182833Erstellt: 25. Oktober 2026

trans-beta-Bromostyrene → trans-Stilbene

https://huagongshe.com/reaction/2182833

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttrans-beta-BromostyreneHCID 5314126—
EduktHCID 178506617HCID 178506617—
KatalysatorPalladiumHCID 23938—
KatalysatorBis(dibenzylideneacetone)palladiumHCID 9811564—
LösungsmittelAcetonitrileHCID 6342—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelPerfluorohexaneHCID 9639—
Produkttrans-StilbeneHCID 638088—

Reaktionsschritte

In an illustrative example, a coupling reaction was conducted between (E)-2-bromostyrene (PhCH═CHBr) and phenylzinc iodide (PhZnI) promoted by a fluorous palladium catalyst. The catalyst was prepared from Pd2(dba)3 and the known fluorous phosphine (p-C6F13CH2CH2C6H4)3P. A mixture of the catalyst in FC-72 was contacted in a U-tube with a first organic phase containing (E)-2-bromostyrene in acetonitrile and a second organic phase containing phenylzinc iodide in THF. After one day at ambient temperature, each organic phase was removed and subjected to standard aqueous workup. Unreacted (E)-2-bromostyrene was recovered from the first organic phase while the coupled reaction product, (E)-stilbene (PhCH═CHPh) was isolated from the second organic phase.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06897331B2
Quelldatensatzuspto-grants-2005_05
ORD IDord-4807387aed194981af52ac32c94e23b4
Quellennotizuspto-grants-2005_05