HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 53725566, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 53775232 | HCID 53775232 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 53725566 | HCID 53725566 | 52.5% |
Reaction Steps
A stirred solution of 5-(3-chloropropyl)-3-phenylmethyleneamino-2-oxazolidinone (2.7 g, 0.0101 mole), dimethylformamide (75 ml) and piperidine (2.15 g, 0.0253 mole, 2.5 eq.) is heated to reflux. Reflux is maintained for 2 hours. After cooling, the solution is concentrated under reduced pressure to a solid-oily residue. This residue is suspended in H2O (200 ml) then extracted with ethyl acetate (3×100 ml). The ethyl acetate is dried over MgSO4, filtered, then concentrated under reduced pressure to an oily-solid residue. This residue is triturated in hexane by stirring 1 hours. The solid is collected and air-dried giving 1.67 g (0.0053 mole) of 3-phenylmethyleneamino-5-[3-(1-piperidinyl)propyl]-2-oxazolidinone.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05994354 |
| Source dataset | uspto-grants-1999_11 |
| ORD ID | ord-87eaf92f827c48d9bbc51b6a12512261 |
| Source note | uspto-grants-1999_11 |