HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropyl Ether → 4-[[O-[N-Methyl-N-(methylthiosulfenyl)carbamoyl]oximino]]-5-methyl-1,3-oxathiolane
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-methyl-N-(methylthiosulfenyl) carbamoyl fluoride | HCID 20479042 | — |
| Reactant | N-(5-Methyl-1,3-oxathiolan-4-ylidene)hydroxylamine | HCID 71364792 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-[[O-[N-Methyl-N-(methylthiosulfenyl)carbamoyl]oximino]]-5-methyl-1,3-oxathiolane | HCID 53951383 | 1.9% |
Reaction Steps
To a solution of 4.22 g (0.032 m) of 5-methyl-4-oximino-1,3-oxathiolane and 5.0 g (0.032 m) of N-methyl-N-(methylthiosulfenyl) carbamoyl fluoride in 25 ml of dioxane was added 3.25 g (0.032 m) of triethylamine. After stirring at room temperature for 19 hrs. the reaction mixture was quenched with 100 ml of water and extracted in ethyl acetate. After the usual work-up it yielded a residual oil. Addition of isopropyl ether resulted in the precipitation of 0.16 g of a solid biscarbamate. The concentrated filtrate was purified by column chromatography to yield 2.97 g of an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232035 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-344b732e97e94e248037819139cdc6ee |
| Source note | uspto-grants-1980_11 |