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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Bicarbonate | HCID 516893 | — |
| Reactant | 4'-tert-Butyl-4-chlorobutyrophenone | HCID 2723694 | — |
| Reactant | 4-(1-(4-Fluoro-benzyl)-1h-benzoimidazole-2-carbonyl)-piperidine trifluoroacetic acid salt | HCID 70101665 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-[4-(1,1-dimethylethyl)phenyl]-4-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]carbonyl]-1-piperidinyl]-1-butanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04908372 |
|---|
| Source dataset | uspto-grants-1990_03 |
|---|
| ORD ID | ord-5a049a4edccb465c92d0769bc0c757de |
|---|
| Source note | uspto-grants-1990_03 |
|---|