HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → Ethanimidothioic acid, 2,2,2-trifluoro-N-[[(methylamino)carbonyl]oxy]-, methyl ester, (E)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | HCID 13003317 | HCID 13003317 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Product | Ethanimidothioic acid, 2,2,2-trifluoro-N-[[(methylamino)carbonyl]oxy]-, methyl ester, (E)- | HCID 9577256 | 74% |
Reaction Steps
One drop of triethylamine was added to a mixture of 6.37 g (0.04 mol) of S-methyl (E)-2,2,2-trifluoro-N-hydroxythioacetimidate and 2.28 g (0.04 mol) of methyl isocyanate. An exothermic reaction ensued, and the reaction mixture was cooled in an ice-bath. The reaction mixture solidified on cooling. Recrystallization from ether gave 6.39 g (74% yield) of S-methyl (E)-2,2,2-trifluoro-N-(methylcarbamoyloxy)thioacetimidate as colorless crystals, mp. 83°-85°. Analysis of the isomer prepared in a similar procedure follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04323578 |
| Source dataset | uspto-grants-1982_04 |
| ORD ID | ord-fe57bbd588a144e7b07c5ba85cdac1d1 |
| Source note | uspto-grants-1982_04 |