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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265936Generated: November 2, 2026

Tert-Butyl nitrite → HCID 12709388, compound

https://huagongshe.com/reaction/1265936

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
Reactant2,2,6,6-Tetramethylpiperidin-1-olHCID 549976—
Reactant2-(ALLYLOXY)ANILINEHCID 6486639—
SolventPyridineHCID 1049—
ProductHCID 12709388HCID 1270938863.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06547841B2
Source datasetuspto-grants-2003_04
ORD IDord-5a2ef82932344a8397a402a69881a41c
Source noteuspto-grants-2003_04