Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diethyl Ether | HCID 3283 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 178418558 | HCID 178418558 | — |
| Product | HCID 13071635 | HCID 13071635 | — |
Reaction Steps
A solution of 7.5 g (0.05 mole) of 1,3,4- thiadiazole-2,5-dithiol (DMTD) was stirred in 700 ml of anhydrous ether in a 3-necked round-bottom flask equipped with a thermometer, a reflux condenser, a dropping funnel, and a magnetic stirrer. The solution was maintained at below 25° C. by cooling while 5.9 ml (0.1 mole) of methyl isocyanate and 0.2 ml of triethylamine were added dropwise. The reaction mixture was stirred at 25° C. for 48 hours. The yellow-solid crystals were collected on a filter, washed with ether and dried. The product was 8.2 grams (62 mole % yield) m.p. 162° C., 2,5-bis(N-methylcarbamylthio)-1,3,4-thiadiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04358597 |
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| Source dataset | uspto-grants-1982_11 |
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| ORD ID | ord-239e219573cc424eba6038ac711b3d22 |
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| Source note | uspto-grants-1982_11 |
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