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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627450Generated: November 2, 2026

Triethylamine → HCID 57672929, compound

https://huagongshe.com/reaction/1627450

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-PiperidoneHCID 12665—
ReactantDi-tert-butyl dicarbonateHCID 90495—
ReactantBenzyl 1-aminocyclohexanecarboxylateHCID 15176238—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 57672929HCID 5767292976.3%

Reaction Steps

A solution of 183 mg (1.5 mmol) of N,N-dimethylaminopyridine and 3.50 g (15 mmol) of 1-aminocyclohexanecarboxylic acid phenylmethyl ester in toluene was added to a solution of 3.27 g (15 mmol) of di-t-butyl dicarbonate in 60 ml of toluene, and the mixture was stirred at room temperature for 30 minutes. Thereafter, 3.04 g (30 mmol) of triethylamine, 1.83 g (15 mmol) of N,N-dimethylaminopyridine and 1.56 g (15.8 mmol) of 2-piperidone were added to the reaction mixture, and the mixture was heated under reflux overnight. Ethyl acetate was added to the reaction solution, and the mixture was successively washed with water, a 10% aqueous potassium hydrogensulfate solution, a saturated aqueous sodium hydrogencarbonate solution and saturated brine, followed by drying with anhydrous sodium sulfate. The solvent was distilled off under reduced pressure and the obtained residue was purified by silica gel chromatography to obtain 4.10 g (76%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785631B2
Source datasetuspto-grants-2014_07
ORD IDord-4fd421f2b70848608b7829510066a8dc
Source noteuspto-grants-2014_07