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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | 4-Nitrobenzyl mercaptan | HCID 193619 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Hydroxy(4-(((4-(hydroxy(oxido)amino)benzyl)dithio)methyl)phenyl)azane oxide | HCID 334132 | 84.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05663164 |
|---|
| Source dataset | uspto-grants-1997_09 |
|---|
| ORD ID | ord-e17c81c55ff74ae89c414eac75229852 |
|---|
| Source note | uspto-grants-1997_09 |
|---|