HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419702Generated: October 29, 2026
Ammonium Chloride → HCID 178420116, compound
https://huagongshe.com/reaction/419702
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Tert-butyl 4-[(2-oxo-2-phenylethyl)carbamoyl]piperidine-1-carboxylate | HCID 58270705 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178420116 | HCID 178420116 | 64% |
Reaction Steps
Microwave heat a mixture of tert-butyl 4-(2-oxo-2-phenylethylcarbamoyl)-piperidine-1-carboxylate (1.0 g, 2.88 mmol) and NH4Cl (0.462 g, 8.65 mmol) in ethanol (12 mL) at 300 W, 160° C., and 14 bar for 11 h in a Personal Chemistry microwave. Cool the mixture to room temperature, add silica gel (5 mL), and concentrate the mixture in vacuo. Purify the residue by silica gel chromatography (80 g RediSep column, elute with a gradient of 0% through 100% CMA/methylene chloride over 60 min, 60 mL/min) to provide 4-(4-phenyl-1H-imidazol-2-yl)piperidine (0.418 g, 64%) as an off-white solid. Add 4-(4-phenyl-1H-imidazol-2-yl)piperidine (0.060 g, 0.26 mmol) to methylene chloride (15 mL) and concentrated hydrochloric acid (28 μL). Stir the mixture for 45 min, then concentrate the mixture in vacuo to provide 4-(4-phenyl-1H-imidazol-2-yl)piperidine hydrochloride (0.070 g, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08093383B2 |
|---|
| Source dataset | uspto-grants-2012_01 |
|---|
| ORD ID | ord-5f8b2bdf243540cabc6864a559303136 |
|---|
| Source note | uspto-grants-2012_01 |
|---|