HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosgene → 1-(1-Benzylpiperidin-4-yl)-3-phenylimidazolidin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | N~1~-(1-Benzylpiperidin-4-yl)-N~2~-phenylethane-1,2-diamine | HCID 20540168 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Potassium Hydroxide | HCID 14797 | — |
| Product | 1-(1-Benzylpiperidin-4-yl)-3-phenylimidazolidin-2-one | HCID 15572668 | 66.4% |
Reaction Steps
With stirring, 15 g of phosgene are introduced at 5° to 10° C in the course of 1 hour into a suspension of 10 g of 1-benzyl-4-(2-phenylamino-1-ethylamino)-piperidine in 100 ml of toluene and 48.5 ml of 3N potassium hydroxide solution. After stirring for 2 hours at 5° to 10° C, the reaction mixture is made alkaline with 43 ml of 6N potassium hydroxide solution and brought to room temperature. After it has been stirred for a further 15 hours at room temperature, the reaction mixture is filtered with suction and the residue is recrystallised from isopropanol-methanol to yield 7.2 g of 1-(1-benzyl-4-piperidinyl)-3-phenyl-2-imidazolidinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04144344 |
| Source dataset | uspto-grants-1979_03 |
| ORD ID | ord-73b45104871d4af5acea485a79c12950 |
| Source note | uspto-grants-1979_03 |