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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1723874Generated: October 25, 2026

2-Propylpiperidine → 4-(2-Propyl-piperidin-1-yl)-butyronitrile

https://huagongshe.com/reaction/1723874

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PropylpiperidineHCID 9985—
ReactantPotassium CarbonateHCID 11430—
Reactant4-BromobutyronitrileHCID 21412—
ReactantDichloromethane methanolHCID 21226129—
SolventAcetonitrileHCID 6342—
SolventSodium chloride; waterHCID 57417360—
Product4-(2-Propyl-piperidin-1-yl)-butyronitrileHCID 1862632283%

Reaction Steps

A mixture of 2-propylpiperidine (550 mg, 4.3 mmol), 4-bromobutyronitrile (430 mg, 3.0 mmol) and potassium carbonate (550 mg, 4.0 mmol) in acetonitrile (5 mL) was stirred at rt for 12 h., followed by addition of a saturated brine (25 mL). The reaction mixture was extracted with ethyl acetate (3×25 mL) and the combined organic phases were dried (MgSO4) and evaporated to dryness to produce crude 8. The crude product was subjected to CC [eluent: CH2Cl2: MeOH (99: 1)] to give pure 8 (0.48 g, 83%); LC-MS [M+H]+ 194 (cald. 194.2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07485651B2
Source datasetuspto-grants-2009_02
ORD IDord-bc522ddd6f44485c9a1863fa5aae7e5b
Source noteuspto-grants-2009_02