Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 429612Erstellt: 24. Oktober 2026

Styrene → trans-Stilbene

https://huagongshe.com/de/reaction/429612

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktStyreneHCID 7501—
Edukt3-BromoquinolineHCID 21413—
EduktSodium AcetateHCID 517045—
KatalysatorTetraphenylphosphonium ChlorideHCID 164911—
LösungsmittelDimethylformamideHCID 6228—
Produkt1,1-DiphenylethyleneHCID 1074014,1%
Produkt3-BromoquinolineHCID 21413—
Produkttrans-StilbeneHCID 63808885,1%
Produktcis-StilbeneHCID 53567850,8%

Reaktionsschritte

A reaction is performed as described in Example 1, except that 3.9 mg (0.015 mmol) of (CH2CN)2PdCl2, 34.9 mg (0.09 mmol) of Ph4PCl, 496.0 mg (6.05 mmol) of anhydrous sodium acetate, 638.74 mg (3.07 mmol) of 3-bromoquinoline and 427.0 mg (4.1 mmol) of styrene are reacted in 1.5 ml of DMF. Stirring is performed at 130° C. for 5 hours. According to the processing described in Example 1, a 72.5% yield of Heck products (85.1% trans-stilbene, 0.8% cis-stilbene, and 14.1% 1,1-diphenylethene) is obtained with 78.5% conversion of 3-bromoquinoline.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06316675B1
Quelldatensatzuspto-grants-2001_11
ORD IDord-dd08380619e74406b89f84d676a720ba
Quellennotizuspto-grants-2001_11