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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520296Generated: November 2, 2026

Ethyl 4-bromobenzoate → HCID 117840693, compound

https://huagongshe.com/reaction/1520296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 4-bromobenzoateHCID 22043—
ReactantBippyPhosHCID 11547931—
ReactantSodium t-butoxideHCID 23676156—
ReactantHCID 117840145HCID 117840145—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
ProductHCID 117840693HCID 117840693—

Reaction Conditions

Temperature70 °C

Reaction Steps

Under a nitrogen atmosphere, a mixture of 4,4,4-trifluoro-1-(5-phenylpyridin-2-yl)butan-1-amine (125.1 mg) obtained in step E, ethyl 4-bromobenzoate (0.214 mL), tris(dibenzylideneacetone)dipalladium (82 mg), 5-(di-tert-butylphosphino)-1′,3′,5′-triphenyl-1′H-[1,4′]bipyrazole (90 mg), sodium tert-butoxide (129 mg), tert-butanol (2.008 mL) and water (0.223 mL) was stirred at 70° C. overnight. To the reaction mixture was added water at room temperature, and the insoluble material was filtered off through celite. The filtrate was extracted with ethyl acetate, and the extract was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was fractionated by HPLC(C18, mobile phase: water/acetonitrile (10 mM ammonium hydrogencarbonate-containing system)). The solvent was evaporated under reduced pressure, and the residue was extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure to give the title compound (35.3 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073864B2
Source datasetuspto-grants-2015_07
ORD IDord-5eb160c3375349f3b2b54218448b5a67
Source noteuspto-grants-2015_07