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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2229739Generated: October 25, 2026

2,2'-Bipyridine → Butyl Acrylate

https://huagongshe.com/reaction/2229739

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,2'-BipyridineHCID 1474—
ReactantMethyl AcrylateHCID 7294—
ReactantEthyl AcetateHCID 8857—
ReactantAllyl 2-bromo-2-methylpropionateHCID 4524555—
Catalystcopper(I) bromideHCID 24593—
SolventAcetonitrileHCID 6342—
ProductButyl AcrylateHCID 8846—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a 30 mL pyrex tube were added methyl acrylate (5 mL, 4.78 g, 55.5 mmole), allyl 2-methyl-2-bromopropionate(0.354 mL, 460 mg, 2.2 mmole), copper (I) bromide (318 mg, 2.22 mmole), 2,2′-bipyridyl (1.04 g, 6.66 mmole), ethyl acetate (4 mL) and acetonitrile (1 mL). The mixture was degassed by three freeze-pump-thaw cycles and then sealed. The mixture was heated to 80° C. for 3 hours and then after cooling to ambient temperature, the mixture was diluted with ethyl acetate (20 mL). An insoluble precipitate was filtered off and the filtrate was washed twice with dil. HCl and once with NaCl solution. The organic layer was dried over Na2SO4 and concentrated under reduced pressure to yield a poly(butyl acrylate) having an alkenyl group at one end and a bromine atom at the other end (3.93 g, 75%). The molecular weight and the molecular weight distribution of the polymer were found to be 2700 and 1.48, respectively, by GPC analysis (based on polystyrene standard). The number of alkenyl groups introduced into the polymer was 0.81 based on 1H NMR analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06420492B1
Source datasetuspto-grants-2002_07
ORD IDord-0b9633905b5348ae89795faf0aef7063
Source noteuspto-grants-2002_07