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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1376852Generated: October 30, 2026

Iodine → Hydroxy(4-(((4-(hydroxy(oxido)amino)benzyl)dithio)methyl)phenyl)azane oxide

https://huagongshe.com/reaction/1376852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
Reactant4-Nitrobenzyl mercaptanHCID 193619—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHydroxy(4-(((4-(hydroxy(oxido)amino)benzyl)dithio)methyl)phenyl)azane oxideHCID 33413284.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

1.0 g of p-nitrobenzylmercaptan was dissolved in 30 of methylene chloride and 0.83 ml of triethylamine and 750 mg of iodine were added while maintaining the temperature at 25° C. and stirring for 10 minutes. After washing with N hydrochloric acid, the organic phase was dried and the solvent was evaporated. 20 ml of ether were added to the residue, and after stirring for 10 minutes, separating and drying, 839 mg of p-nitrobenzyl disulfide melting at 126° C. were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05663164
Source datasetuspto-grants-1997_09
ORD IDord-e17c81c55ff74ae89c414eac75229852
Source noteuspto-grants-1997_09