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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1457219Generated: November 3, 2026

Citric Acid → 1,1-Dimethylethyl 3,3-dimethyl-2-oxo-1-piperidinecarboxylate

https://huagongshe.com/reaction/1457219

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantMethyl iodideHCID 6328—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactanttert-Butyl 2-oxopiperidine-1-carboxylateHCID 7577838—
SolventDiethyl EtherHCID 3283—
SolventTetrahydrofuranHCID 8028—
Product1,1-Dimethylethyl 3,3-dimethyl-2-oxo-1-piperidinecarboxylateHCID 57267608—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To the title compound of Step (A) (1.08 g, 5.42 mmol) in 10.8 ml THF at -78° C., lithium bis(trimethylsilyl)amide (1M in THF, 13.6 ml, 13.6 mmol) was added dropwise in 10 min. The mixture was stirred at -78° C. for 30 minutes and methyl iodide (4.62 g, 32.52 mmol) was added. The reaction mixture was slowly warmed to room temperature and stirred at room temperature for two days. To the reaction mixture, 30 ml Et2O and 15 ml 5% aqueous citric acid were added. The organic liquid was separated and washed with 10 ml 5% citric acid, H2O, brine and dried and concentrated. The residue was chromatographed on silica gel using 19:1 hexane/EtOAc to give the title compound of this step (440 mg, 38%) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05846990
Source datasetuspto-grants-1998_12
ORD IDord-408b8951bf974325b04a01a5404ac5ea
Source noteuspto-grants-1998_12