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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546745Generated: October 30, 2026

tert-Butyl methacrylate → HCID 66839446, compound

https://huagongshe.com/reaction/546745

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl methacrylateHCID 11448—
ReactantTri-o-tolylphosphineHCID 80271—
ReactantSodium AcetateHCID 517045—
ReactantHCID 86628513HCID 86628513—
CatalystPalladium, di-mu-chlorobis(eta3-2-propenyl)di-HCID 61538—
SolventTolueneHCID 1140—
SolventDimethylacetamideHCID 31374—
ProductHCID 66839446HCID 66839446—

Reaction Steps

A mixture of 6-chloro-2-methoxy-3-(4-methyl-1H-imidazol-1-yl)pyridine (400 mg), an allylpalladium chloride dimer (32.8 mg), tri-o-tolylphosphine (54.4 mg), sodium acetate (441 mg), dimethylacetamide (0.640 mL), tert-butyl methacrylate (0.724 mL) and toluene (2 mL) was stirred in a nitrogen atmosphere at 120° C. for 3.5 hours. The reaction solution was left to cool to room temperature. Then, a silica gel was added and the reaction solution was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (elution solvent: heptane-ethyl acetate system) to obtain 313 mg of tert-butyl (E)-3-[6-methoxy-5-(4-methyl-1H-imidazol-1-yl)pyridin-2-yl]-2-methylacrylate. The ester was diluted with trifluoroacetic acid (2.48 mL) and methylene chloride (2.48 mL), and the reaction solution was stirred at room temperature for 3.5 hours. The reaction solution was concentrated under reduced pressure to obtain 260 mg of the title compound. The property value of the compound is as follows.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07935815B2
Source datasetuspto-grants-2011_05
ORD IDord-1a6ccff7f5344086a8c634df1131230c
Source noteuspto-grants-2011_05