Ethanol → 5-Norbornene 2-allylacetate 5-butylnorbornene

HRID 1160023

Reaktionsgleichung

[CH:1]12[CH2:7][CH:4]([CH:5]=[CH:6]1)[CH2:3][CH2:2]2.[CH2:8]([CH2:11][C:12]([O-:14])=[O:13])[CH:9]=[CH2:10].[CH2:15]([CH:19]1[CH2:24][CH:23]2[CH2:25][CH:20]1[CH:21]=[CH:22]2)[CH2:16][CH2:17][CH3:18].C1(C)C=CC=CC=1.C(O)C>C(Cl)Cl.CC([O-])=O.CC([O-])=O.[Pd+2]>[CH:1]12[CH2:7][CH:4]([CH:3]=[CH:2]1)[CH2:5][CH2:6]2.[CH2:8]([CH2:11][C:12]([O-:14])=[O:13])[CH:9]=[CH2:10].[CH2:15]([CH:19]1[CH2:24][CH:23]2[CH2:25][CH:20]1[CH:21]=[CH:22]2)[CH2:16][CH2:17][CH3:18]

Komponenten

Reaktionsbedingungen

Temperatur: 90 °C

Versuchsvorschrift

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.

Aufarbeitung

additionadded to the monomer solution
additionto dilute it
customto precipitate a white polymer, which
filtrationwas filtered through a glass funnel
washwashed with ethanol
customdried in vacuo at 80° C. for 24 hours

Quellen und Nachweise

ORD-Eintrag: ord-d61723dacc474dc480954dcbdb26e9bd
Quelldatensatz: uspto-grants-2010_10
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US07814713B2

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