Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2200144Generated: October 26, 2026

Cesium carbonate → 4-Fluoro-1-(3-nitro-5-(trifluoromethyl)phenyl)piperidine

https://huagongshe.com/reaction/2200144

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant4-Fluoropiperidine hydrochlorideHCID 2759158—
Reactant1-Bromo-3-nitro-5-(trifluoromethyl)benzeneHCID 7015411—
CatalystBinap, (A+-)-HCID 634876—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
Product4-Fluoro-1-(3-nitro-5-(trifluoromethyl)phenyl)piperidineHCID 9002061263.4%

Reaction Conditions

Temperature100 °C

Reaction Steps

Mix 1-bromo-3-nitro-5-(trifluoromethyl)benzene (700 mg, 2.59 mmol), 4-fluoropiperidine hydrochloride (544 mg, 3.89 mmol), cesium carbonate (2.5 g, 7.77 mmol), (±)-2,2′-bis(diphenylphosphino)-1,1′-binaphthalene (BINAP, 48 mg, 0.077 mmol), tris(dibenzylideneacetone)dipalladium [Pd2(dba)3, 47 mg, 0.052 mmol] in dioxane (10 mL), Stir the mixture under nitrogen atmosphere at 100° C. for 16 hrs. Cool the reaction mixture to room temperature, dilute it with water (10 mL), extract with ethyl acetate (10 mL×2), combine the organic layers, wash with brine (15 mL) and dry over anhydrous sodium sulfate. Concentrate the filtrate to get the crude product. Purify by flash chromatography (silica gel, 100% PE) to yield the target compound (480 mg, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09359338B2
Source datasetuspto-grants-2016_06
ORD IDord-ad5bb0cf52584ba09693fc092e428a39
Source noteuspto-grants-2016_06