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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 597551Generated: November 1, 2026

Ethanol → HCID 86734587, compound

https://huagongshe.com/reaction/597551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantEthyl bromoacetateHCID 7748—
Reactant4-Hydroxy-2,2,6,6-tetramethylpiperidineHCID 75471—
ProductHCID 86734587HCID 86734587—

Reaction Steps

A mixture of 15.7 parts of 2,2,6,6-tetramethylpiperidin-4-ol and 8.3 parts of ethyl bromoacetate in 50 parts of ethyl alcohol was heated at reflux for 48 hours. The cooled reaction mixture was filtered to remove 2,2,6,6-tetramethylpiperidin-4-ol hydrobromide and the solvent removed by distillation in vacuo. The residue was triturated with 40°-60°C petroleum ether to remove the unreacted 2,2,6,6-tetramethylpiperidin-4-ol. The filtrate was then distilled under reduced pressure to yield pure 1-ethoxy-carbonylmethyl-2,2,6,6-tetramethylpiperidin-4-ol as a colourless liquid (of boiling point 116°C at 0.2 mm) which slowly solidified on standing (melting point 42°-42.5°C). This material gave the following elemental analysis by weight:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04014887
Source datasetuspto-grants-1977_03
ORD IDord-4649275a84894c0f8ace921b2342e252
Source noteuspto-grants-1977_03