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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,2,6,6-tetramethyl-4-hydroxypiperidine-N-oxide | HCID 11607999 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-acetyloxy-2,2,6,6-tetramethylpiperidine-N-oxide | HCID 86671501 | 78.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08912287B2 |
|---|
| Source dataset | uspto-grants-2014_12 |
|---|
| ORD ID | ord-83f334867a4243d1b1b64e626ad8b412 |
|---|
| Source note | uspto-grants-2014_12 |
|---|