HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → HCID 21423225, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | HCID 21423234 | HCID 21423234 | — |
| Reactant | HCID 21423245 | HCID 21423245 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21423225 | HCID 21423225 | — |
Reaction Steps
A solution of 4.8 g. of 1-[p-(methylthio)phenyl]-1H-tetrazole in 80 ml. of methylene chloride was treated with 2.2 ml. of sulfuryl chloride in 10 ml. of methylene chloride. The solution was stirred at room temperature for 1 hour, evaporated to dryness on a steam bath, washed with hexane and recrystallized from methylene chloride to give white crystals, m.p. 115°-117° C. This product was also obtained by a similar reaction of 0.5 g. of 1-[p-(methylsulfinyl)phenyl]-1H-tetrazole and 0.18 ml. of thionyl chloride in methylene chloride.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04036849 |
| Source dataset | uspto-grants-1977_07 |
| ORD ID | ord-ee55f82141b44a63a99fa62f6852f0e8 |
| Source note | uspto-grants-1977_07 |