HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → N-(3-methyl-5-isothiazolyl)-N'-methylurea
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | 3-Methylisothiazol-5-amine | HCID 32307 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(3-methyl-5-isothiazolyl)-N'-methylurea | HCID 23336007 | 54.5% |
Reaction Steps
Methylisocyanate (1.96 milliliters, 0.04 mole) was added dropwise to a thirty (30) milliliter solution of the distilled tetrahydrofuran containing the above mentioned 5-amino-3-methylisothiazole (5.0 grams, 0.04 mole), and then the resulting yellow solution was refluxed for 3 hours, during which time a white precipitate formed. The solution was cooled and filtered, giving 3.73 grams of N-(3-methyl-5-isothiazolyl)-N'-methylurea, also referred to as 3-methyl-5-N-methylureiodisothiazole.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04152516 |
| Source dataset | uspto-grants-1979_05 |
| ORD ID | ord-5292de97bb924efc96de2b966bd65664 |
| Source note | uspto-grants-1979_05 |