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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1992247Generated: October 26, 2026

Ethanol → 5-Norbornene 2-allylacetate 5-butylnorbornene

https://huagongshe.com/reaction/1992247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantTolueneHCID 1140—
ReactantBicyclo[2.2.1]hept-2-ene, 5-butyl-HCID 168020—
Reactant5-Norbornene 2-allylacetateHCID 86597587—
Catalystpalladium(II) acetateHCID 167845—
SolventDichloromethaneHCID 6344—
Product5-Norbornene 2-allylacetate 5-butylnorborneneHCID 86603900—

Reaction Conditions

Temperature90 °C

Reaction Steps

5-norbornene-2-allylacetate (NB-CH2—O—C(O)—CH3) (5 mL, 30.9 mmol), 5-butyinorbornene (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 μmol) and [(Cy)3PH][(B(C6F5)4) (1.48 mg, 1.55 μmol) 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07648937B2
Source datasetuspto-grants-2010_01
ORD IDord-668940ccf75e419285be4bba58566c57
Source noteuspto-grants-2010_01