Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 14576906 | HCID 14576906 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Trifluoroacetic acid | HCID 6422 | — |
| Product | HCID 14576907 | HCID 14576907 | 100.7% |
Reaction Steps
To a solution of 2.5 g of 1-(4-chlorophenyl)-6-(4-methylsulfonylphenyl)-2-piperidone in 10 ml of methylene chloride, 15 ml of anhydrous trifluoroacetic acid was added, and the mixture was refluxed at 45° C. for 3 hours. After cooling, 100 ml of a mixture of methanol and triethylamine (1:1) was added, and the mixture was stirred at room temperature for 1 hour and then treated with a saturated aqueous ammonium chloride solution. The methylene chloride layer was washed with water, dried, and evaporated to give 2.2 g of 1-(4-chlorophenyl)-6-(4-mercaptophenyl)-2-piperidone as pale yellow oily product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04839360 |
|---|
| Source dataset | uspto-grants-1989_06 |
|---|
| ORD ID | ord-8f1f7df4782349be935c78650d69b306 |
|---|
| Source note | uspto-grants-1989_06 |
|---|