HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Aminophenol → 1,2-Benzisoselenazol-3(2H)-one, 2-(4-hydroxyphenyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Aminophenol | HCID 403 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | HCID 22643532 | HCID 22643532 | — |
| Product | 1,2-Benzisoselenazol-3(2H)-one, 2-(4-hydroxyphenyl)- | HCID 3067578 | — |
Reaction Steps
of 4-aminophenol dissolved in 200 cc. of tetrahydrofurane (THF) and 2 cc. of pyridine are added with stirring and ice-cooling (temperature below 10° C.) under a nitrogen atmosphere to a solution of 3.3 g. of o-chloroselenobenzoic acid chloride in 30 cc. of THF. After termination of the addition, the mixture is stirred at room temperatur, the solvent is evaporated under vacuum and the residue is pured into a mixture of ice and dilute hydrochloric acid. The resulting precipitate is filtered off and is recrystallized from ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04418069 |
| Source dataset | uspto-grants-1983_11 |
| ORD ID | ord-3996c9aad54b4c5697d6d3e18db36d1d |
| Source note | uspto-grants-1983_11 |