HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862966Generated: November 1, 2026
Acetonitrile → Triethylammonium 6-ethylpyrid-2-yldithiocarbamate
https://huagongshe.com/reaction/1862966
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | 6-Ethylpyridin-2-amine | HCID 89021 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | Triethylammonium 6-ethylpyrid-2-yldithiocarbamate | HCID 20393066 | — |
Reaction Steps
A solution of carbon disulphide (17.5 cc) in anhydrous acetonitrile (19.5 cc) is added, at 25° C., to a solution of 2-amino-6-ethylpyridine (27.0 g) in anhydrous triethylamine (60 cc). After stirring for 20 hours at 20° C., anhydrous diethyl ether(250 cc) is added. After cooling for 1 hour at 2° C., the resulting crystals are filtered off, washed three times with anhydrous diethyl ether (total 240 cc) and dried under reduced pressure (20 mm Hg) at 20° C. Triethylammonium 6-ethylpyrid-2-yldithiocarbamate (42.0 g), melting at 75° C., is thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04167571 |
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| Source dataset | uspto-grants-1979_09 |
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| ORD ID | ord-463df491162d46ae9c9e0fbd03dda3fd |
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| Source note | uspto-grants-1979_09 |
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