HuagongsheHuagongshe Chemistry Print Report · For research reference only
Chloroacetone → 4-[(2-Oxopropyl)thio]-1-(phenylmethyl)piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Chloroacetone | HCID 6571 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | 1-Benzylpiperidine-4-thiol | HCID 11275783 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-[(2-Oxopropyl)thio]-1-(phenylmethyl)piperidine | HCID 15229280 | — |
Reaction Steps
A suspension of 1-(phenylmethyl)piperidine-4-thiol (70 g, prepared in Example 1), chloroacetone (26.9 ml), sodium carbonate (71.6 g) and tetrabutylammonium iodide (31.2 g) in toluene (350 ml) is stirred at room temperature for 4 hours. The insoluble material is filtered off and washed with toluene. After concentration, the filtrate is taken up in dichloromethane and washed with dilute sodium hydroxide and then with a saturated aqueous solution of sodium chloride. After drying over sodium sulfate, the solution is concentrated to give 4-[(2-oxopropyl)thio]-1-(phenylmethyl)piperidine (82.2 g) in the form of an oil, which is sufficiently pure to be used in the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05418242 |
| Source dataset | uspto-grants-1995_05 |
| ORD ID | ord-0538c0659dca44d59cb3c635b7f6c0bf |
| Source note | uspto-grants-1995_05 |