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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1468295Generated: November 1, 2026

2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane → HCID 86710110, compound

https://huagongshe.com/reaction/1468295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Ethenyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 5233012—
ReactantHCID 86710111HCID 86710111—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
ProductHCID 86710110HCID 8671011070%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-(4,4-Difluorocyclohexylmethyl)-6-iodo-2-trifluoromethylimidazo[1,2-a]pyridine-7-carbonitrile (20.0 mg, 0.0430 mmol) obtained in step 2 was dissolved in 1,2-dichloromethane (0.60 mL), and the solution was stirred at 60° C. for 1 hour after adding 4,4,5,5-tetramethyl-2-vinyl-1,3,2-dioxaborolane (24.0 mg, 0.153 mmol), tetrakis(triphenylphosphine)palladium(0) (4.93 mg, 0.00426 mmol), and water (0.2 mL). The reaction mixture was filtered through Celite (registered trademark), and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate=90/10→50/50) to give 3-(4,4-difluorocyclohexylmethyl)-2-trifluoromethyl-6-vinylimidazo[1,2-a]pyridine-7-carbonitrile (11.0 mg, yield 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000186B2
Source datasetuspto-grants-2015_04
ORD IDord-c4cd555fe1364e89be0fb9566ff65646
Source noteuspto-grants-2015_04