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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1265938Generated: November 2, 2026

Pyridine → HCID 12709388, compound

https://huagongshe.com/reaction/1265938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1,4-Dihydroxy-2,2,6,6-tetramethylpiperidineHCID 5395—
ReactantTert-Butyl nitriteHCID 10906—
Reactant2-(ALLYLOXY)ANILINEHCID 6486639—
SolventChlorobenzeneHCID 7964—
ProductHCID 12709388HCID 1270938859%

Reaction Steps

The procedure of Example 1 is repeated using 1.95 g (12.5 mmol) of 1-oxyl-2,2,6,6-tetramethyl-4-hydroxypiperidine, 3.10 g (30 mmol) of tert-butyl nitrite, 2.4 g (25 mmol) of pyridine, 7.5 mg (0.012 mmol) of (S,S)-(+)-N,N-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) mmol) in 100 mL of chlorobenzene and 5.60 g (25 mmol) of 2-allyloxyaniline in 20 mL of chlorobenzene. The crude product obtained is purified by vacuum flash chromatography (25% ethyl acetate/heptane) to give 2.13 g of a viscous liquid in 59.0% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06547841B2
Source datasetuspto-grants-2003_04
ORD IDord-79dbba16729b48d0a453692619b99e10
Source noteuspto-grants-2003_04