HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2397171Generated: October 27, 2026
Methyl Isocyanate → HCID 178485914, compound
https://huagongshe.com/reaction/2397171
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 178482505 | HCID 178482505 | — |
| Catalyst | 1,4-Dioxane | HCID 31275 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 178485914 | HCID 178485914 | 75.5% |
Reaction Steps
To a stirred slurry of 126 g of 2-methylamino-5-mercapto-1,3,4-thiadiazole in 525 ml of dioxane containing a few drops of triethylamine is added 49 g of methyl isocyanate. After stirring two hours at room temperature, the solid is collected by filtration and washed with hexane giving 165 g, melting at 162°-3°. This product is heated on the steam bath 11/2 -2 hours with 250 ml of triethylamine, during which time the initial solid is converted to a heavy amber oil. The supernatent liquid is decanted and the oil is dissolved in water and neutralized with dilute hydrochloric acid to pH 2-3. The precipitated solid is collected and washed with water and air dried, giving 132 g of N,N'-dimethyl-N'-(5-mercapto-1,3,4-thiadiazol-2-yl)urea, m.p. 230° (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04021225 |
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| Source dataset | uspto-grants-1977_05 |
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| ORD ID | ord-28f568c20bb949ddb94ba26cb4c1b498 |
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| Source note | uspto-grants-1977_05 |
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