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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1817324Generated: October 26, 2026

2-Piperidone → 1-(3-Chloro-4-fluorobenzyl)piperidin-2-one

https://huagongshe.com/reaction/1817324

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PiperidoneHCID 12665—
ReactantSodium hydrideHCID 24758—
Reactant4-(Bromomethyl)-2-chloro-1-fluorobenzeneHCID 2757542—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product1-(3-Chloro-4-fluorobenzyl)piperidin-2-oneHCID 66997683—

Reaction Conditions

Temperature0 °C

Reaction Steps

Valerolactam (153.3 g, 1.54 mol) was dissolved in NMP (3.5 L) and cooled to 0° C. NaH (67.7 g, 1.69 mol, 60% dispersion in oil) was added in portions over 5 minutes keeping the temperature at 0° C. The reaction was stirred for 30 minutes, and 3-chloro-4-fluorobenzylbromide (345.5 g, 1.54 mol) dissolved in 200 mL NMP was added over 30 minutes, again keeping the internal temperature at 0° C. The reaction was aged for 1 hour at 0° C., and allowed to warm to room temperature overnight. LCMS showed the reaction complete. The reaction mixture was quenched with 5 L distilled H2O, extracted with 3 portions of CH2Cl2 (2 L, 1 L, 1 L) and the organic layers combined and washed with three 4 L portions of water. The organic layer was concentrated and was found to contain NMP. The residual oil was dissolved in EtOAc (4 L), and extracted with three 2 L portions of water. The organic layer was concentrated to give the product that solidified upon standing.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07598264B2
Source datasetuspto-grants-2009_10
ORD IDord-cbdda365d198445081464a8a5464edfe
Source noteuspto-grants-2009_10