HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265936Generated: November 2, 2026
Tert-Butyl nitrite → HCID 12709388, compound
https://huagongshe.com/reaction/1265936
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 2,2,6,6-Tetramethylpiperidin-1-ol | HCID 549976 | — |
| Reactant | 2-(ALLYLOXY)ANILINE | HCID 6486639 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 12709388 | HCID 12709388 | 63.7% |
Reaction Steps
To a solution of 1.95 g (12.5 mmol) of 1-oxyl-2,2,6,6-tetramethylpiperidine, 3.1 g (30 mmol) of tert-butyl nitrite and 7.5 mg (0.012 mmol) of (S,S)-(+)-N,N-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) in 100 mL of pyridine at 65°-70° C. under a nitrogen atmosphere is added dropwise over 20 minutes a solution of 5.6 g (25 mmol) of 2-allyloxyaniline in 20 mL of pyridine. The evolution of gas is observed during the addition of the 2-allyloxyaniline. After the addition is complete, the reaction mixture is kept at 65°-70° C. for an additional forty minutes until gas evolution subsided. After cooling to ambient temperature, the reaction mixture is then concentrated. The residue obtained is purified by vacuum flash chromatography (heptane) to give 2.3 g of a viscous liquid in 63.7% yield. The structure is confirmed by 1Hnmr and elemental analyses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06547841B2 |
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| Source dataset | uspto-grants-2003_04 |
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| ORD ID | ord-5a2ef82932344a8397a402a69881a41c |
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| Source note | uspto-grants-2003_04 |
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