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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434447Generated: October 25, 2026

Sebacoyl chloride → Bis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacate

https://huagongshe.com/reaction/434447

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSebacoyl chlorideHCID 66072—
Reactant4-Piperidinol, 1,2,2,6,6-pentamethyl-HCID 75472—
Reactant1,2,2,6,6-Pentamethylpiperidin-4-ol hydrochlorideHCID 20492522—
SolventBenzeneHCID 241—
ProductBis(1,2,2,6,6-pentamethyl-4-piperidyl) sebacateHCID 586744—

Reaction Steps

A solution of 17.10 parts of 1,2,2,6,6-pentamethylpiperidin-4-ol in 50 parts of dry benzene was stirred at 15°-20° C. whilst adding 6.0 parts of sebacoyl chloride dropwise over 15 minutes. The mixture was stirred for a further 12 hours at room temperature after which the 1,2,2,6,6-pentamethylpiperidin-4-ol hydrochloride formed during the reaction was filtered off. The benzene was removed by distillation under reduced pressure to give a yellow oil, which was distilled under reduced pressure to give bis-(1,2,2,6,6-pentamethyl-4-piperidinyl)sebacate as a colourless oil having a boiling point of 218°-20° C. at 0.4 mm of Hg and the following elemental analysis by weight:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE031343
Source datasetuspto-grants-1983_08
ORD IDord-ec8fa515ba964b79a3f62dde5080d7b7
Source noteuspto-grants-1983_08