Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 4-Nitroaniline | HCID 7475 | — |
| Reactant | 4-Hydroxy-2,2,6,6-tetramethylpiperidine | HCID 75471 | — |
| Reactant | Sodium Tetrafluoroborate | HCID 4343483 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 87132637 | HCID 87132637 | 4.6% |
Reaction Steps
A mixture of concentrated HCl (15 ml, 32%) and water (15 ml) is charged into 100 ml three necked round bottomed flask followed by addition of 4-nitro-aniline (5 g, 0.04 mol). The mixture is cooled to 0 to 5° C. and solution of sodium nitrite (4.14 g, 0.06 mol) in water (5 ml) is added into it while maintaining temperature 0 to 5° C. This reaction mixture is then slowly added into a solution of sodium tetrafluoroborate (6.6 g, 0.06 mol) in water (60 ml) at 0 to 5° C. The resulting solution of diazonium tetrafluoroborate salt is then added to solution of 2,2,6,6-tetramethyl-4-hydroxypiperdine (25.1 g, 0.16 mol) in acetonitrile (1000 ml)) and the mixture is stirred at 0 to −5° C. for 1 h. This reaction mixture filtered and mother liquor is evaporated to dryness at 40° C. The residue is extracted with diethyl ether (200 ml) the extract is decolorized with charcoal (50 g), filtered through bed of celite and concentrated to dryness to afford 0.56 g of 2,2,6,6-Tetramethyl-1-(4-nitrophenyldiazenyl)-piperidin-4-ol as a yellow solid, m.p. 108-110° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08940806B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-f248639eff0c4e679ae25a27e52a7aca |
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| Source note | uspto-grants-2015_01 |
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