Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1604291Generated: November 1, 2026

Piperidine → HCID 53725566, compound

https://huagongshe.com/reaction/1604291

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantHCID 53775232HCID 53775232—
SolventDimethylformamideHCID 6228—
ProductHCID 53725566HCID 5372556652.5%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05994354
Source datasetuspto-grants-1999_11
ORD IDord-87eaf92f827c48d9bbc51b6a12512261
Source noteuspto-grants-1999_11