HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(4-Benzyloxy-phenyl)-5-trifluoromethyl-1H-tetrazole → 4-(5-Trifluoromethyl-tetrazol-1-YL)-phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(4-Benzyloxy-phenyl)-5-trifluoromethyl-1H-tetrazole | HCID 21197251 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(5-Trifluoromethyl-tetrazol-1-YL)-phenol | HCID 21197249 | 99.8% |
Reaction Steps
A solution of 1(4-benzyloxy-phenyl)-5-trifluoromethyl-1H-tetrazole (45.3 mmol) in ethanol (100 ml) and tetrahydrofuran (100 ml) was hydrogenated at room temperature and atmospheric pressure over 10% palladium-carbon catalyst (6 g). After 2 h, the mixture was filtered and the filtrate was evaporated to give the title compound (10.4 g) as a cream solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06020346 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-94e770b933f340a89e072179f906a8dd |
| Source note | uspto-grants-2000_02 |