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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 379085Generated: November 1, 2026

Triethylamine → Benzyl 2-(4-oxopiperidin-1-yl)acetate

https://huagongshe.com/reaction/379085

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPotassium CarbonateHCID 11430—
Reactant4-PiperidoneHCID 33721—
ReactantHCID 9991399HCID 9991399—
SolventAcetoneHCID 180—
ProductBenzyl 2-(4-oxopiperidin-1-yl)acetateHCID 1818798983%

Reaction Steps

To a stirred suspension of 4-piperidone (10.0 g, 65.0 mmol) and bromobenzyl acetate (14.9 g, 65.2 mmol) in acetone (100 ml) was added K2CO3 (9.0 g) and Et3N (9.1 ml, 65.2 mmol). The reaction mixture was stirred at room temperature for two days, and then the solvent was evaporated. The residue was partitioned between EtOAc and water. The aqueous layer was extracted with EtOAc. The organic extracts were combined and dried over Na2SO4. The solvent was evaporated to afford the title compound (13.3 g, 53.8 mmol, 83%) as a thick oil. 1H NMR (300 MHz, CDCl3) δ 7.33-7.37 (m, 5H), 5.18 (s, 2H), 3.42 (s, 2H), 2.91 (t, J=6.1 Hz, 4H), 2.50 (t, J=6.1 Hz, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297260B1
Source datasetuspto-grants-2001_10
ORD IDord-935551db6865440b9ffada4c72ee8ce8
Source noteuspto-grants-2001_10