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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095389Generated: November 1, 2026

Butyl Acrylate → HCID 68185504, compound

https://huagongshe.com/reaction/2095389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButyl AcrylateHCID 8846—
Reactanttert-Butyl peroxybenzoateHCID 11966—
ReactantN-TriisopropylsilylpyrroleHCID 145136—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventHCID 86642677HCID 86642677—
ProductHCID 68185504HCID 68185504133.5%

Reaction Conditions

Temperature35 °C

Reaction Steps

Palladium(II) acetate (0.05 equiv.) was added to a solution of n-butyl acrylate (0.27 mL, 1.5 mmol, 0.50 equiv.), 1-(triisopropylsilyl)-1H-pyrrole (1.34 g, 3.00 mmol), and tert-butyl peroxybenzoate (0.56 mL, 1.5 mmol, 0.50 equiv.), in acetic acid/dioxane/dimethylsulfoxide (0.23/0.69/0.08 mL). The mixture was stirred at 35° C. for 24 h, diluted with diethyl ether (200 mL) and water (20 mL), and filtered through a plug of celite. The organic phase was separated and washed with saturated NaHCO3 solution (2×30 mL) and water (30 mL). The combined aqueous layers were further extracted with CH2Cl2. The combined organic extracts were dried over MgSO4, filtered, and concentrated in vacuo. The residue was purified by CC (SiO2, EtOAc/petroleum ether 1:20) to give (E)-butyl 3-[1-(triisopropylsilyl)-1H-pyrrol-3-yl]acrylate (0.70 g, 67%) as a light-yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445684B2
Source datasetuspto-grants-2013_05
ORD IDord-97472cde517343538cc8de56267ca16b
Source noteuspto-grants-2013_05