| Chemical Name | Nitrosoniumtetrafluoroborate |
| Synonym |
四氟硼酸亚硝
tetrafluoro-borate(1-nitrosyl
Nitrosonium fluoroborate
Nitrosoniumtetrafluoroborate98%
nitrosium tetrafluoroborate
NITROSYL TETRAFLUOROBORATE
Nitrosonium tetrafluoroborate, min. 97%
Nitrosoniumtetrafluoroborate,min.97%
NITROSONIUM (NITROSYL) TETRAFLUOROBORATE
NITROSONIUM TETRAFLUOROBORATE
Nitrosonium tetrafluoroborate 98% |
| MDL Number | MFCD00011433 |
| PubChem Substance ID | 24850360 |
| EC Number | 238-679-2 |
| CAS Number | 14635-75-7 |
| Merck Number | 14,6649 |
| Beilstein Registry Number | 2384789 |
| Chemical Name Translation | 亚硝鎓四氟硼酸盐 |
{ALF} With excess reagent, oxidation of the isoxazoline to the isoxazole occurs.
{ALF} Undergoes an interesting insertion reaction with diarylcyclopropanes: Chem. Lett., 233 (1988):
{ALF}
{ALF} Crystalline nitrosating agent: Secondary amines to nitrosamines: Chem. Ber., 89, 2374 (1956); deamination of primary amides: J. Org. Chem., 30, 2386 (1965); conversion of arylhydrazines to azides: Tetrahedron Lett., 28, 5091 (1987). In organic solvents, converts arylamines directly to diazonium tetrafluoroborates which undergo the Balz-Schiemann reaction (see Tetrafluoroboric acid, L14037) in situ to give high yields of aryl fluorides: Chem. Ber., 88, 1939 (1955); EP 430,434 (1991). Methyl or methoxy substituted aromatics in acetonitrile give the nitrosoaromatics in good yield: J. Org. Chem., 59, 5573 (1994).
{ALF} Convenient catalyst for iodination of aromatics by iodide ion with air as oxidant: J. Org. Chem., 53, 3548 (1988), or for addition of iodine (or iodine + nucleophile) to alkenes: Acta Chem. Scand. B, 43, 902 (1989).