HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2225902Generated: October 31, 2026
Sodium Thiosulfate → HCID 54543206, compound
https://huagongshe.com/reaction/2225902
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | Aluminum Sulfate | HCID 24850 | — |
| Reactant | Sodium Dichromate | HCID 25408 | — |
| Reactant | HCID 19438635 | HCID 19438635 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 54543206 | HCID 54543206 | 89.3% |
Reaction Steps
N-(4-Ethoxycarbonylbutyl)-N-methyl-p-phenylenediamine (1.7 g) was dissolved in 1N hydrochloric acid (13.6 ml) and to the solution was added a solution of aluminium sulfate 14-18 hydrate in water (10 ml). The mixture was ice-cooled. A solution of sodium thiosulfate 5 hydrate (2 g) in water (8 ml) was added thereto and further a solution of sodium dichromate 2 hydrate (0.798 g) in water (5 ml) was added dropwise. The resulting mixture was stirred for 30 minutes under ice-cooling. Then acetic acid (0.6 ml) was added and the mixture was further stirred at room temperature for 2 hours. The reaction mixture was concentrated to dryness. The concentrate was made alkaline with an aqueous sodium bicarbonate and insoluble materials were filtered off. The filtrate was adjusted to pH 4 with acetic acid, concentrated to about 50 ml and cooled. The resulting crystalline precipitate was filtered off, washed with cold water and dried to obtain the desired compound (2.1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05344928 |
|---|
| Source dataset | uspto-grants-1994_09 |
|---|
| ORD ID | ord-9e4c24a8d21041e6a59f1dbb6f5869cd |
|---|
| Source note | uspto-grants-1994_09 |
|---|