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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 464762Generated: October 27, 2026

Toluene → 1,4-Dihydro-2,6-dimethyl-4-oxo-1-(2,2,6,6-tetramethyl-4-piperidinyl)3-pyridinecarboxylic acid

https://huagongshe.com/reaction/464762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
Reactant4-Amino-2,2,6,6-tetramethylpiperidineHCID 37524—
ReactantDehydroacetic acidHCID 122903—
SolventWaterHCID 962—
Product1,4-Dihydro-2,6-dimethyl-4-oxo-1-(2,2,6,6-tetramethyl-4-piperidinyl)3-pyridinecarboxylic acidHCID 20262552—

Reaction Steps

A 1-liter, 3-neck, round-bottom flask was equipped with a mechanical stirrer, thermometer, and a Dean-Stark water trap topped with a water cooled condenser. The flask was charged with a mixture of 80.5 g (0.479 mol) dehydroacetic acid, 75.0 g (0.479 mol) 4-amino-2,2,6,6-tetramethylpiperidine, and 600 ml toluene. The stirred mixture in the flask was heated to the boiling point by means of an oil bath and the water formed during the reaction was collected in the trap. After 6 hours of reflux a total of 7.0 ml water had been collected and the flask and its contents cooled to room temperature. The mixture deposited crystals on standing which were collected by vacuum filtration. Reduction of volume of toluene in the filtrate caused a deposit of a second crop of crystals. The combined crystals were recrystallized from a 65/35 mixture of hexane/benzene to give 111 g (75.6%) of a white to colorless crystalline solid (M.P. 174° C.). The chemical structure and purity of these crystals were verified by mass spectroscopy, nuclear magnetic resonance spectroscopy; and by elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04548973
Source datasetuspto-grants-1985_10
ORD IDord-466c70680aab4535acc032aff1d4c2e8
Source noteuspto-grants-1985_10