HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 45550Generated: October 29, 2026
4-(4-Chlorophenyl)-4-(4-iodophenyl)piperidine → 4-[4-(4-Chlorophenyl)piperidin-4-yl]benzonitrile
https://huagongshe.com/reaction/45550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-(4-Chlorophenyl)-4-(4-iodophenyl)piperidine | HCID 59331974 | — |
| Reactant | HCID 178418546 | HCID 178418546 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-[4-(4-Chlorophenyl)piperidin-4-yl]benzonitrile | HCID 67235769 | 16% |
Reaction Steps
A mixture of 4-(4-chloro-phenyl)-4-(4-iodo-phenyl)-piperidine and copper (I) cyanide in DMF was heated at 140° C. under nitrogen for 6 hours then allowed to cool. The mixture was diluted with ethyl acetate, washed with a mixture of conc. ammonia and brine (×5), dried (MgSO4), filtered and concentrated to give a residue which was partially purified by column chromatography (SiO2), eluting with a gradient of 2M ammonia in methanol (5% to 10%) and dichloromethane to afford the title compound (46 mg, <16%). This was taken on to the next reaction without further purification. LCMS (PS-A2) Rt 2.39 min [M+H]+ 297.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541461B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-405089bbec3246eca80f37f976315643 |
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| Source note | uspto-grants-2013_09 |
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