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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 856028Generated: October 30, 2026

Ethyl Acetate → 4-[4-(Tert-butyldimethylsiloxy)piperidin-1-yl]benzonitrile

https://huagongshe.com/reaction/856028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantBenzonitrile, 4-bromo-HCID 12162—
Reactant4-((Tert-butyldimethylsilyl)oxy)piperidineHCID 11481328—
ReactantSodium t-butoxideHCID 23676156—
Catalystpalladium(II) acetateHCID 167845—
CatalystBinap, (A+-)-HCID 634876—
SolventTolueneHCID 1140—
Product4-[4-(Tert-butyldimethylsiloxy)piperidin-1-yl]benzonitrileHCID 6948052866%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 4-bromobenzonitrile (2.76 g, 15.16 mmol), 4-(tert-butyldimethylsiloxy)piperidine (2.9 g, 13.79 mmol), palladium acetate (62 mg, 0.28 mmol), (S)-(−)-2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP) (258 mg, 0.41 mmol), and sodium tert-butoxide (1.99 g, 20.68 mmol) in toluene (60 ml) was stirred at 80° C. for 1 hour. The reaction mixture was allowed to return to room temperature, to which ethyl acetate (60 ml) was added, and the mixture was filtered. The filtration was washed with water and brine, and dried over magnesium sulfate. After filtration, the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (n-hexane/methylene chloride=1/1) to afford 4-[4-(tert-butyldimethylsiloxy)piperidin-1-yl]benzonitrile (2.8 g, yield 66%) as a pale yellow crystalline powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07262212B2
Source datasetuspto-grants-2007_08
ORD IDord-b2a554d3b81b49d48178e13bc701e6cc
Source noteuspto-grants-2007_08