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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1710152Generated: October 31, 2026

Triethylamine → HCID 22153826, compound

https://huagongshe.com/reaction/1710152

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Oxo-2-phenylacetyl chlorideHCID 11084294—
ReactantHCID 19991754HCID 19991754—
SolventDichloromethaneHCID 6344—
ProductHCID 22153826HCID 2215382676%

Reaction Conditions

Temperature-10 °C

Reaction Steps

24.1 g (0.1 mole) of 4-hexyloxy-2,2,6,6-tetramethylpiperidine are dissolved in 100 ml of absolute methylene chloride. To this solution are added 15.2 g (0.15 mole) of absolute triethylamine and the whole solution is cooled to -10° C. At this temperature a solution of 16.8 g (0.1 mole) of phenylglyoxylyl chloride in 100 ml of methylene chloride is slowly added dropwise. When this addition is complete, the reaction mixture is allowed to warm to room temperature and stirred for about 4 hours. Precipitated hydrochloride is removed by filtration and the solution is clarified by filtration over a small amount of silica gel and concentrated by evaporation, affording 28.4 g of 1-(4-hexyloxy-2,2,6,6-tetramethylpiperidino)-2-phenyl-ethane-1,2-dione as a yellow oil (stabiliser 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04952620
Source datasetuspto-grants-1990_08
ORD IDord-5694b658392f45f6a07e629df628c163
Source noteuspto-grants-1990_08