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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1436931Generated: November 3, 2026

Acetonitrile → HCID 69064282, compound

https://huagongshe.com/reaction/1436931

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantPotassium CarbonateHCID 11430—
Reactant5-Fluoro-2-(trifluoromethyl)benzyl bromideHCID 2737578—
Reactanttert-Butyl (3S)-3-[(propan-2-yl)amino]pyrrolidine-1-carboxylateHCID 53346612—
SolventEthyl AcetateHCID 8857—
ProductHCID 69064282HCID 69064282—

Reaction Steps

A solution of 1,1-dimethylethyl (3S)-3-[(1-methylethyl)amino]pyrrolidine-1-carboxylate (0.34 g, 1.5 mmol) and 2-(trifluoromethyl)-5-fluorobenzyl bromide (0.58 g, 2.25 mmol) in acetonitrile (5 mL) was heated at reflux with anhydrous potassium carbonate (0.41 g, 3 mmol) for 24 hours. The reaction mixture was cooled, diluted with ethyl acetate and washed with water. The organic extracts were washed with brine, dried (MgSO4), filtered and evaporated in vacuo to give an oil. This was purified by flash chromatography on silica, eluting with ethyl acetate/cyclohexane (0:100 to 10:90), to give the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07619096B2
Source datasetuspto-grants-2009_11
ORD IDord-548bddb55514412eb9b58a507f2fe27a
Source noteuspto-grants-2009_11