HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → triethylammonium N-(2-pyrazinyl)-dithiocarbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Aminopyrazine | HCID 78747 | — |
| Solvent | Hexane | HCID 8058 | — |
| Product | triethylammonium N-(2-pyrazinyl)-dithiocarbamate | HCID 19962701 | 31.6% |
Reaction Steps
In a 100-ml flask, 4.9 g (50 mmol) of 3-aminopyrazine, 4.5 g (59 mmol) of carbon disulfide and 50 ml of ethyl acetate were placed, and 6.5 g (64 mmol) of triethylamine was added dropwise with stirring over a 5-min period on a water bath. After the mixture was stirred at 60° C. for 5 hr. 10 ml of hexane was added to the mixture, which was allowed to stand overnight at room temperature to precipitate yellow crystals. The crystals were separated from the solution by filtration, and washed with 5 ml of ethyl acetate to obtain 4.3 g of triethylammonium N-(2-pyrazinyl)-dithiocarbamate (Intermediate II-1). Yield 31%. Mp 113°-116° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616456 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-44ea6459c73449988937bfaeef87df1a |
| Source note | uspto-grants-1997_04 |