HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 1,3-Dithiolan-2-one, O-((((1,1-dimethylethyl)dithio)methylamino)carbonyl)oxime
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Oximino-1,3-dithiolane | HCID 12404078 | — |
| Reactant | N-methyl-N-(tert-butylthiosulfenyl)carbamoyl fluoride | HCID 20399612 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1,3-Dithiolan-2-one, O-((((1,1-dimethylethyl)dithio)methylamino)carbonyl)oxime | HCID 3059608 | — |
Reaction Steps
2-[[O-[N-Methyl-N-(tert-butylthiosulfenyl)carbamoyl]oximino]]-1,3-dithiolane was prepared according to the procedure described in Example I, by reacting 2.9 g (0.0214 m) of 2-oximino-1,3-dithiolane, 4.23 g (0.0214 m) of N-methyl-N-(tert-butylthiosulfenyl)carbamoyl fluoride and 2.17 g (0.0214 m) of triethylamine in 50 ml of dioxane. 2-[[O-[N-Methyl-N-tert-butylthiosulfenyl)carbamoyl]oximino]]-1,3-dithiolane crystallized from methylene chloride isopropyl ether to yield 4.0 g of a white solid. It was then recrystallized from ethyl acetate to yield a solid, m.p. 112°-114° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232035 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-badd9a2a625a4508953c96755c87c88a |
| Source note | uspto-grants-1980_11 |