HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bis(3-nitrophenyl) disulfide → HCID 13044799, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bis(3-nitrophenyl) disulfide | HCID 10842 | — |
| Reactant | Chlorine | HCID 24526 | — |
| Reactant | Sulfur dichloride | HCID 25353 | — |
| Reactant | P-Tolyl vinyl sulfone | HCID 79665 | — |
| Reactant | 1-(Chlorosulfanyl)-3-nitrobenzene | HCID 15620686 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Product | HCID 13044799 | HCID 13044799 | — |
Reaction Steps
A solution of 0.642 mole of m-nitrobenzenesulfenyl chloride in enough carbon tetrachloride to make 1060 ml was prepared by passing chlorine for 6.5 hours into a solution of 99 g (0.321 mole) of bis(m-nitrophenyl)disulfide in 1 liter of carbon tetrachloride at 45° C. One-quarter of this solution (265 ml, equivalent to 0.161 mole of the sulfenyl chloride) was treated with 29.2 g (0.160 mole) of p-tolyl vinyl sulfone. Upon standing for several weeks crystals separated. Filtration gave 18 g (30%) of crude product m.p. 92°-101°. Recrystallization from 30 ml of ethyl acetate gave pure material m.p. 103.5°-104.5°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04335142 |
| Source dataset | uspto-grants-1982_06 |
| ORD ID | ord-ca90ad2d36bf456aab287682b4124388 |
| Source note | uspto-grants-1982_06 |