HuagongsheHuagongshe Chemistry Print Report · For research reference only
Lawesson's reagent → 1-(4-Aminophenyl)piperidine-2-thione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Lawesson's reagent | HCID 87949 | — |
| Reactant | 1-(4-Aminophenyl)piperidin-2-one | HCID 11458178 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 1-(4-Aminophenyl)piperidine-2-thione | HCID 12114408 | — |
Reaction Steps
2.1 15 g (78.8 mmol) of 1-(4-aminophenyl)piperidin-2-one are heated to the boil together with 16.0 g (39.5 mmol) of 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide (Lawesson's reagent) in 100 ml of anhydrous toluene. After 45 minutes, the solvent is evaporated, and the residue is taken up in dichloromethane and 2 N HCl. The aqueous phase is extracted three times with dichloromethane and adjusted to a pH of 12 using conc. NaOH. Extraction with dichloromethane, drying over sodium sulfate and evaporation of the solvent give 1-(4-aminophenyl)piperidine-2-thione as a colourless solid, ESI 207.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07566789B2 |
| Source dataset | uspto-grants-2009_07 |
| ORD ID | ord-faa337e8e4724e26b55acdd5ced85869 |
| Source note | uspto-grants-2009_07 |