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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357818Generated: November 4, 2026

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

https://huagongshe.com/reaction/1357818

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 numberUS06593347B2
Source datasetuspto-grants-2003_07
ORD IDord-19382dd0516b4020b3c499ed83fcd020
Source noteuspto-grants-2003_07