HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tert-Butyl nitrite → HCID 22598266, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | 2,4-Dibromoaniline | HCID 12004 | — |
| Reactant | 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 | HCID 69964483 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 22598266 | HCID 22598266 | 43.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06579328B2 |
| Source dataset | uspto-grants-2003_06 |
| ORD ID | ord-bed2c163f60f4dbcbaa1d123d982a0b9 |
| Source note | uspto-grants-2003_06 |