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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1160023Erstellt: 26. Oktober 2026

Ethanol → 5-Norbornene 2-allylacetate 5-butylnorbornene

https://huagongshe.com/reaction/1160023

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthanolHCID 702—
EduktTolueneHCID 1140—
EduktBicyclo[2.2.1]hept-2-ene, 5-butyl-HCID 168020—
Edukt5-Norbornene 2-allylacetateHCID 86597587—
Katalysatorpalladium(II) acetateHCID 167845—
LösungsmittelDichloromethaneHCID 6344—
Produkt5-Norbornene 2-allylacetate 5-butylnorborneneHCID 86603900—

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

5-norbornene-2-allylacetate (NB—CH2—O—C(O)—CH3) (5 mL, 30.9 mmol), 5-butylnorbornene (1.3 mL, 7.7 mmol), and toluene (7.3 mL) were charged into a 250 mL Schlenk flask. Pd(OAc)2 (0.17 mg, 0.77 p mol) and [(Cy)3PH][(B(C6F5)4) (1.48 mg, 1.55 p mol) were dissolved in CH2Cl2 (1 mL) and added to the monomer solution. While the reaction mixture was stirred for 18 hours at 90° C., the reaction mixture became viscous. After the reaction was completed, 120 ml of toluene was added to the viscous solution to dilute it. The solution was poured into an excess of ethanol to precipitate a white polymer, which was filtered through a glass funnel, washed with ethanol, and dried in vacuo at 80° C. for 24 hours to yield 5-norbornene-2-allylacetate/5-butylnorbornene copolymer (4.35 g: 69.2% by weight based on the total weight of used monomers). The weight average molecular weight (Mw) of the copolymer was 303,550 and Mw/Mn was 2.16.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07814713B2
Quelldatensatzuspto-grants-2010_10
ORD IDord-d61723dacc474dc480954dcbdb26e9bd
Quellennotizuspto-grants-2010_10