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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369349Generated: November 2, 2026

Tert-Butyl nitrite → HCID 22598266, compound

https://huagongshe.com/reaction/1369349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-Butyl nitriteHCID 10906—
Reactant2,4-DibromoanilineHCID 12004—
Reactant2,4-bis[N-butyl-N-(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)amino]-6-[N,N-bis(2-ethylhexyl)amino]-s-triazineHCID 69964483—
SolventPyridineHCID 1049—
ProductHCID 22598266HCID 2259826643.4%

Reaction Steps

The procedure of Example 1 is repeated using 10 g (13 mmol) of 2,4-bis[N-butyl-N-(1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl)amino]-6-[N,N-bis(2-ethylhexyl)amino]-s-triazine, 6.18 g (60 mmol) of tert-butyl nitrite, 7.8 mg (0.013 mmol) of (S,S)-(+)-N,N-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II), 140 mL of pyridine and 13.05 g (52 mmol) of 2,4-dibromoaniline at 85° C. The crude product obtained is purified by vacuum flash chromatography (2% ethyl acetate/heptane) to give 7 g of the title compound as a light yellow solid in 43.4% yield. The structure is confirmed by 1Hnmr and elemental analysis.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06579328B2
Source datasetuspto-grants-2003_06
ORD IDord-bed2c163f60f4dbcbaa1d123d982a0b9
Source noteuspto-grants-2003_06