HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → 2-Phenylbenzenesulfonyl isothiocyanate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | HCID 13422022 | HCID 13422022 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Phenylbenzenesulfonyl isothiocyanate | HCID 13422027 | 54.6% |
Reaction Steps
77 g of potassium N-(2-biphenylylsulfonyl)carbonimidodithioate were suspended in 100 ml of toluene, and 37 ml of thionyl chloride were added dropwise at 0° to 10° C. over the course of 1 hour. After the addition, the mixture was stirred at room temperature for 2 hours. The reaction mixture was filtered, and the filtrate was concentrated under reduced pressure and distilled under reduces pressure to give 30 g of 2-phenylbenzenesulfonyl isothiocyanate represented by the following formula: ##STR27##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04568381 |
| Source dataset | uspto-grants-1986_02 |
| ORD ID | ord-09f6ba9830a04a03a6293dc869439c9b |
| Source note | uspto-grants-1986_02 |