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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Piperidone | HCID 12665 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 4-(Bromomethyl)-2-chloro-1-fluorobenzene | HCID 2757542 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-(3-Chloro-4-fluorobenzyl)piperidin-2-one | HCID 66997683 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07598264B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-cbdda365d198445081464a8a5464edfe |
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| Source note | uspto-grants-2009_10 |
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