HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → 2-(2-hydroxy-5-methylphenyl)benztriazole N-oxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Azobenzene | HCID 2272 | — |
| Reactant | Fluorenone | HCID 10241 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 4-Methyl-2-[2-(2-nitrophenyl)diazenyl]phenol | HCID 74029 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(2-hydroxy-5-methylphenyl)benztriazole N-oxide | HCID 13214646 | — |
Reaction Steps
95% potassium hydroxide 17.7 g was added and dissolved in a mixture of ethyl alcohol 80 ml and water 10 ml. 2-nitro-2'-hydroxy-5'-methylazobenzene 12.9 g was then added to the resultant solution at 50° to 60° C. for 30 minutes while stirring, and thereafter 9-fluorenone 0.6 g and 35% formalin 5.6 g were added to the solution in 30 minutes. The resultant mixture was stirred for 1 hour at 65° to 70° C., and was further reacted at the boiling point (85° C.) for 4 hours, thus almost all of the azobenzene having disappeared to produce 2-(2-hydroxy-5-methylphenyl)benzotriazole-N-oxide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04780541 |
| Source dataset | uspto-grants-1988_10 |
| ORD ID | ord-4601cd0a238a42dbb3c6dd0150e027b6 |
| Source note | uspto-grants-1988_10 |