HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → N-(5,5,7,7-Tetramethyl-4,5,6,7-tetrahydrobenzothiazol-2-YL)-N'-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | Isocyanate | HCID 105034 | — |
| Reactant | 4,5,6,7-tetrahydro-5,5,7,7-tetramethyl-2-Benzothiazolamine | HCID 12783348 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(5,5,7,7-Tetramethyl-4,5,6,7-tetrahydrobenzothiazol-2-YL)-N'-methylurea | HCID 12783349 | — |
Reaction Steps
2-Amino-5,5,7,7-tetramethyl-4,5,6,7-tetrahydrobenzothiazole (21 grams; 0.1 mole) was dissolved in ethyl acetate (100 ml) and the solution charged into a glass reaction vessel fitted with a mechanical stirrer and themometer. Methyl isocyanate (6.2 grams 0.11 mole) was added dropwise to this solution over a period of 30 minutes. The temperature of the reactants was at about 20°-25° C. during the addition. At the conclusion of the isocyanate addition, stirring was continued at room temperature for a period of about 2 hours. The desired product, 2-amino-5,5,7,7-tetramethyl-4,5,6,7-tetrahydrobenzothiazole, a solid, was then filtered from the reaction mixture and air dried. Its melting point was greater than 250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04289524 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-19c871d1ec5f49a3b2e5bf323111be6b |
| Source note | uspto-grants-1981_09 |