HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → Tinuvin
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-(2-hydroxy-3-t-butyl-5-methylphenyl)-5-chlorobenzotriazole-N-oxide | HCID 14149470 | — |
| Solvent | Water | HCID 962 | — |
| Product | Tinuvin | HCID 62531 | 82.9% |
Reaction Steps
In order to conduct the reaction of Process (c), the system was heated, and was stirred at 66° to 68° C. (boiling point) for 5 hours. As this result, the N-oxide disappeared, thus Process (c) being completed. Thereafter, water 50 ml was added to the reaction liquor, and the resultant reaction liquor was neutralized with 62% sulfuric acid 10 g to precipitate a crystal. The precipitated crystal was separated by filtration, and the separated crystal was fully washed with hot water of 60° to 70° C. and further with a small amount of methanol. The washed crystal was then dried, thus obtaining 8.7 g of 2-(2'-hydroxy-3'-t-butyl-5'-methylphenyl)-5-chlorobenzotriazole having a melting point of 138° to 140° C. at the yield of 82.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04835284 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-b87118cb457540f9b227a12747cf0e34 |
| Source note | uspto-grants-1989_05 |