HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → 4-(1H-1,2,3,4-tetrazol-1-yl)phenol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | Sodium Azide | HCID 33557 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 4-(1H-1,2,3,4-tetrazol-1-yl)phenol | HCID 542910 | 30% |
Reaction Steps
To a stirred solution of p-amino-phenol (0.1 mol) in glacial acetic acid (140 ml) at 70-75° under nitrogen atmosphere was added triethylorthoformate (0.1 mol). The mixture was stirred at this temperature for 4 h, then, sodium azide (0.32 mol) was added portionwise and the reaction was continued for 18 h, cooled to room temperature and poured into ice water (400 ml) and extracted with diethyl ether (3×400 ml) and ethyl acetate (1×400 ml), dried (MgSO4), filtered and concentrated to give a dark brown residue which was triturated with 200 ml of a mixture of ethanol:diethyl ether (1:1 v/v) and filtered to afford the title compound in 30% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06020346 |
| Source dataset | uspto-grants-2000_02 |
| ORD ID | ord-53f140dcf3da4e959a2ab144e43febf6 |
| Source note | uspto-grants-2000_02 |