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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192245Generated: October 30, 2026

Piperidine → 2-[2-Hydroxy-3-(1-piperidinyl)propyl]-1H-isoindole-1,3(2H)-dione

https://huagongshe.com/reaction/1192245

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantN-(2,3-Epoxypropyl)phthalimideHCID 21601—
SolventEthanolHCID 702—
Product2-[2-Hydroxy-3-(1-piperidinyl)propyl]-1H-isoindole-1,3(2H)-dioneHCID 6020746370.8%

Reaction Steps

To a solution of 2-(oxiran-2-ylmethyl)isoindoline-1,3-dione (1.0 g, 4.9 mmol) in ethanol (25 mL) was added piperidine (0.46 g, 5.4 mmol). The resulting reaction mixture was heated at reflux for 1 hour. After this time, TLC analysis showed no starting material remaining so the mixture was concentrated to afford the title product as oil (1.0 g). The titled product structure was confirmed by LC/MS analysis. MS m/z: 289.21 [M+H]+. The resulting hydroxylamine was dissolved in ethanol (20 mL) and to which was added hydrazine (0.86 g, 7.36 mmol). The resulting reaction mixture was stirred at ambient temperature for over night. After this time, TLC analysis showed no starting material remaining so the mixture was concentrated to afford the title product as oil (0.4 g). MS m/z: 159.2 [M+H]+. The crude was used as such for the next step transformation.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680139B2
Source datasetuspto-grants-2014_03
ORD IDord-7463f035e82d4032920755a3cd8eff55
Source noteuspto-grants-2014_03