HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 5-Chloro-3-(ethylsulfanyl)-1,2,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Trichloromethanethiol | HCID 6390 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | HCID 178419564 | HCID 178419564 | — |
| Product | 5-Chloro-3-(ethylsulfanyl)-1,2,4-thiadiazole | HCID 23079390 | — |
Reaction Steps
To 60 ml of water, 10.3 g of ehtylisothiourea hydrobromide, 10.4 g of perchloromethylmercaptan were added, followed the solution of 9.39 g of sodium hydroxide dissolved to 60 ml of water was added dropwise slowly at about 0° C. Then, t-butylmethylether was added to the reaction mixture, and extracted. The organic layer was dried by anhydrous sodium salfate, and concentrated. The residue obtaind was subjected to silica gel column chromatography (hexanne:ethylacetate=30:1) to obtain 2.54 g of 3-ethylthio-5-chloro-1,2,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07342031B2 |
| Source dataset | uspto-grants-2008_03 |
| ORD ID | ord-93036e25438b436287b77393ef266a3f |
| Source note | uspto-grants-2008_03 |