HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Disulfide → Dibutyldithiocarbamic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | Dibutylamine | HCID 8148 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | Dibutyldithiocarbamic acid | HCID 8685 | — |
Reaction Steps
5′-(Dibutyldithiocarbamyl)-2,5-dimercapto-1,3,4-thiadiazole (i.e., formula (I) where X is hydrogen and R1 and R2 are n-butyl radicals) was prepared in the following manner. In 100 grams of isopropyl alcohol 26 grams of dibutyl amine was combined with 16 grams of CS2 and held at a temperature of about 40° C. for about 1 hour to yield a dibutyl dithiocarbamic acid intermediate. Subsequently, 30 grams of 2,5-dimercapto-1,3,4-thiadiazole was added to the mixture along with 20 grams of 35 wt. % hydrogen peroxide. The mixture was reacted for about 1 hour at a temperature of about 28° C. to yield the liquid end product 5′-(dibutyldithiocarbamyl)-2,5-dimercapto-1,3,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06635696B1 |
| Source dataset | uspto-grants-2003_10 |
| ORD ID | ord-6790862ded7b49eea72d2feb6c86f4b1 |
| Source note | uspto-grants-2003_10 |