HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N-(1-phenylcyclohexyl)trimethylacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 1-Phenylcyclohexylamine | HCID 31862 | — |
| Reactant | Pivaloyl chloride | HCID 62493 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | N-(1-phenylcyclohexyl)trimethylacetamide | HCID 12879909 | 63.3% |
Reaction Steps
Into a 200 ml four-necked flask, there were charged toluene (150 ml), 1-phenylcyclohexylamine (10.5 g) and pyridine (5.2 g), and trimethylacetyl chloride (7.2 g) was dropwise added thereto while stirring at room temperature. Stirring was continued for 3 hours. After completion of the reaction, the reaction mixture was washed with water to remove pyridine hydrochloride. The toluene layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was recrystallized from ethanol to give 9.8 g of N-(1-phenylcyclohexyl)trimethylacetamide. M.P., 129°-130.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04270002 |
| Source dataset | uspto-grants-1981_05 |
| ORD ID | ord-409925d5de8540908842b44436f77fdb |
| Source note | uspto-grants-1981_05 |