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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1649535Generated: October 31, 2026

4-Aminophenol → 1,2-Benzisoselenazol-3(2H)-one, 2-(4-hydroxyphenyl)-

https://huagongshe.com/reaction/1649535

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminophenolHCID 403—
ReactantPyridineHCID 1049—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 22643532HCID 22643532—
Product1,2-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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04418069
Source datasetuspto-grants-1983_11
ORD IDord-3996c9aad54b4c5697d6d3e18db36d1d
Source noteuspto-grants-1983_11