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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171756Generated: November 3, 2026

Pyrrolidine → HCID 68766810, compound

https://huagongshe.com/reaction/1171756

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyrrolidineHCID 31268—
ReactantTert-butyl 3-oxopyrrolidine-1-carboxylateHCID 471360—
ReactantEthyl (4-formyl-1H-pyrazol-1-yl)acetateHCID 53491200—
SolventEthanolHCID 702—
ProductHCID 68766810HCID 6876681035%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 1-(t-butoxycarbonyl)pyrrolidin-3-one (6.8 g) in ethanol (200 ml) were added ethyl(4-formyl-1H-pyrazol-1-yl)acetate (8.0 g) and pyrrolidine (600 μl). The resulting mixture was stirred at 80° C. for 45 minutes, cooled to room temperature, and the solvent was evaporated in vacuo. The residue was purified by chromatography on silica gel using a mixture of hexane, ethyl acetate and dichloromethane (2:1:1) as the eluent to afford the title compound as a yellow amorphous solid (4.47 g, yield: 35%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829580B2
Source datasetuspto-grants-2010_11
ORD IDord-e0beed6f4e304f088a5126da10ca4542
Source noteuspto-grants-2010_11