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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1165213Generated: October 27, 2026

Potassium Iodide → 1-[4-(1,1-dimethylethyl)phenyl]-4-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]carbonyl]-1-piperidinyl]-1-butanone

https://huagongshe.com/reaction/1165213

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium BicarbonateHCID 516893—
Reactant4'-tert-Butyl-4-chlorobutyrophenoneHCID 2723694—
Reactant4-(1-(4-Fluoro-benzyl)-1h-benzoimidazole-2-carbonyl)-piperidine trifluoroacetic acid saltHCID 70101665—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
Product1-[4-(1,1-dimethylethyl)phenyl]-4-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]carbonyl]-1-piperidinyl]-1-butanoneHCID 19800499—

Reaction Steps

[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]-4-piperidinylmethanone mono (trifluoroacetate) (5.0 g, 11 mmol), 4-chloro-4'-tert-butylbutyrophenone (6.2, 26 mmol), potassium bicarbonate (2.5 g, 25 mmol), and potassium iodide (catalytic amount) were combined and refluxed in toluene (50 ml) and water (5 ml) for 3 days. The cooled layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water, brine, dried (MgSO4), and concentrated. The resulting oil was chromatographed on silica gel (75×160 mm), eluting with ethyl acetate. The appropriate fractions were combined, concentrated, and the resulting oil crystallized from cyclohexane to afford 1-[4-(1,1-dimethylethyl)phenyl]-4-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]carbonyl]-1-piperdinyl]-1-butanone: 3.4 g (57%), m.p. 105°-106° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04908372
Source datasetuspto-grants-1990_03
ORD IDord-5a049a4edccb465c92d0769bc0c757de
Source noteuspto-grants-1990_03