HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfuric Acid → Phenol, 2-(2H-benzotriazol-2-yl)-4-(1,1-dimethylethyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Anthrone | HCID 7018 | — |
| Reactant | (2R,3S,4R,5R)-2,3,4,5,6-pentahydroxyhexanal | HCID 107526 | — |
| Reactant | 2-(2-hydroxy-5-t-butylphenyl)benzotriazole-N-oxide | HCID 13907172 | — |
| Catalyst | Fluorenone | HCID 10241 | — |
| Product | Phenol, 2-(2H-benzotriazol-2-yl)-4-(1,1-dimethylethyl)- | HCID 76605 | — |
Reaction Steps
9-fluorenone 0.7 g was then added to the reaction liquor thus obtained, and the liquor was heated to 55°~60° C. Thereafter, glucose 6.0 g was added to the reaction liquor over 30 minutes, and the reaction was conducted at 75° C. (boiling point) for 6 hours. As this result, the N-oxide disappeared, thus Process (c) being completed. Thereafter, pH of the reaction liquor was made to 8 with 62% sulfuric acid 19.0 g to precipitate a crystal. The precipitated crystal was separated by filtration, and the separated crystal was fully washed with water and further with methanol. The washed crystal was then dried, thus obtaining 11.6 g of 2-(2'-hydroxy-5'-t-butylphenyl)benzotriazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04835284 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-3effd731557643d5ad8e4a40f09dab5c |
| Source note | uspto-grants-1989_05 |