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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429218Generated: November 2, 2026

Ethyl Acrylate → HCID 66629898, compound

https://huagongshe.com/reaction/1429218

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcrylateHCID 8821—
ReactantTri-tert-butylphosphine tetrafluoroborateHCID 2734635—
ReactantBis(cyclohexylmethyl)amineHCID 4594378—
ReactantHCID 58226548HCID 58226548—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66629898HCID 6662989883%

Reaction Conditions

Temperature60 °C

Reaction Steps

To (S)-tert-butyl 2-(5-bromo-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-benzo[d]imidazol-2-yl)pyrrolidine-1-carboxylate (2.973 g, 5.99 mmol), ethyl acrylate (0.714 mL, 6.59 mmol), tri-tert-butylphosphonium tetrafluoroborate (0.104 g, 0.359 mmol), N,N-dicyclohexylmethylamine (1.461 mL, 6.89 mmol), and tris(dibenzylideneacetone)dipalladium(0) (0.164 g, 0.18 mmol) dissolved in THF (18 mL) had nitrogen bubbled through the solution for 15 minutes to remove the oxygen, and then the mixture heated at 60° C. for 2 hours. After cooling to room temperature the solution was filtered through diatomaceous earth and washed with EtOAc. The filtrated was then concentrated to a residue, and then the residue was dissolved in dichloromethane and extracted with water. The organic layer was then dried and concentrated. The residue was purified by chromatography (silica gel, hexanes in ethyl acetate) which afforded 2.56 g, (83%) of the title compound. MS (ESI) m/z 516 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08937150B2
Source datasetuspto-grants-2015_01
ORD IDord-7180f3e37a9149ee94b0de3b8cd37a71
Source noteuspto-grants-2015_01