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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404314Generated: November 1, 2026

Acetic Anhydride → 4-acetyloxy-2,2,6,6-tetramethylpiperidine-N-oxide

https://huagongshe.com/reaction/1404314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
Reactant2,2,6,6-tetramethyl-4-hydroxypiperidine-N-oxideHCID 11607999—
SolventTetrahydrofuranHCID 8028—
Product4-acetyloxy-2,2,6,6-tetramethylpiperidine-N-oxideHCID 8667150178.5%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution in which 30.3 g (300 mmol) of triethylamine and 34.4 g (200 mmol) of 4-hydroxy-2,2,6,6-tetramethylpiperidine-N-oxide (TEMPOL) were dissolved in 200 mL of tetrahydrofuran (THF), 25.5 g (250 mmol) of acetic anhydride was added at 0° C. The temperature was raised to 25° C. to carry out a reaction for 12 hours, and it was then concentrated by a rotary evaporator. The residue was supplied to 1 liter of iced water, and the precipitated orange solid was collected by filtration to obtain 33.8 g of 4-acetyloxy-2,2,6,6-tetramethylpiperidine-N-oxide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912287B2
Source datasetuspto-grants-2014_12
ORD IDord-83f334867a4243d1b1b64e626ad8b412
Source noteuspto-grants-2014_12