HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → N-(5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)-N'-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 2-Amino-5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazole | HCID 20548472 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | N-(5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)-N'-methylurea | HCID 20569296 | — |
Reaction Steps
2-Amino-5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazole (0.1 mole) is dissolved in ethyl acetate (100 ml) and the solution is charged into a glass reaction vessel fitted with a stirrer and thermometer. Methyl isocyanate (0.11 mole) is added dropwise to this solution over a period of about 30 minutes. The temperature of the reactant is held at about 20° C. to 30° C. during the addition. At the end of the addition, stirring is continued at room temperature for a period of about 2 hours. The reaction mixture is then filtered and the filtered-off solids are air dried to yield the desired product N-(5,5,7-trimethyl-4,5,6,7-tetrahydrobenzothiazol-2-yl)-N'-methylurea.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04289524 |
| Source dataset | uspto-grants-1981_09 |
| ORD ID | ord-7777590c1fce48ce85448ca03943b192 |
| Source note | uspto-grants-1981_09 |