HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → 2,4-Di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | (+-)-2-Butanol | HCID 6568 | — |
| Reactant | Tributylamine | HCID 7622 | — |
| Reactant | Phenol, 2-(2-(4-chloro-2-nitrophenyl)diazenyl)-4,6-bis(1,1-dimethylethyl)- | HCID 104112 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2,4-Di-tert-butyl-6-(5-chloro-2H-benzotriazol-2-yl)phenol | HCID 77470 | 78.6% |
Reaction Steps
39.0 g (0.1 mol) of 2-nitro-4-chloro-2'-hydroxy-3',5'-di-t-butylazobenzene, 0.125 g of 5% palladium carbon, 100 ml of toluene, 60 ml of 2-butanol, 120 ml of water and 7 g of tributylamine were charged into a 500-ml stainless autoclave with an agitator. Reaction was effected in the same manner as that employed in Example 1. After the reaction had been completed, after treatment was performed in the same way as that employed in Example 1 to obtain 28.1 g of 2-(2'-hydroxy-3',5'-di-t-butylphenyl)-5-chlorbenzotriazole(yield, 78.6%; melting point, 152° to 153° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05187289 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-ee668654c7394118aef8cf47221195d3 |
| Source note | uspto-grants-1993_02 |