HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-[(3,4-Dichlorophenyl)sulfanyl]-5-(trifluoromethyl)-1,3,4-thiadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 3,4-Dichlorobenzenethiol | HCID 79964 | — |
| Reactant | 2-Bromo-5-(trifluoromethyl)-1,3,4-thiadiazole | HCID 12874685 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-[(3,4-Dichlorophenyl)sulfanyl]-5-(trifluoromethyl)-1,3,4-thiadiazole | HCID 54353624 | 76% |
Reaction Steps
130.5 g (0.66 mole) of 2-bromo-5-trifluoromethyl-1,3,4-thiadiazole were added dropwise to a solution of 98.1 g (0.66 mole) of 3,4dichloro-thiophenol and 57.6 g (0.66 mole) of triethylamine in 500 ml of ethanol. An exothermic effect was observed and a white precipitate separated out. The mixture was stirred for a further 2 hours under reflux, concentrated to half in vacuo and introduced into 1 liter of ice water. The white precipitate was filtered off, dried over phosphorus pentoxide and recrystallized from about 300 ml of petroleum ether. 147 g (76% of theory) of 2-(3',4' -dichlorophenylthio)-5-trifluoromethyl-1,3,4-thiadiazole of melting point 46° C were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04097669 |
| Source dataset | uspto-grants-1978_06 |
| ORD ID | ord-67fa17f57c2a4dfcb6a0471ef1a7116b |
| Source note | uspto-grants-1978_06 |