HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pentane → 2-[[O-[N-Methyl-N-(-butylthiosulfenyl)carbamoyl]oximino]]-3,5,5-trimethylthiazolidin-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pentane | HCID 8003 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-(Hydroxyimino)-3,5,5-trimethyl-1,3-thiazolidin-4-one | HCID 71363389 | — |
| Reactant | Butylthiosulfenylcarbamoyl fluoride | HCID 86737314 | — |
| Product | 2-[[O-[N-Methyl-N-(-butylthiosulfenyl)carbamoyl]oximino]]-3,5,5-trimethylthiazolidin-4-one | HCID 53823089 | — |
Reaction Steps
2-[[O-[N-Methyl-N-(-butylthiosulfenyl)carbamoyl]oximino]]-3,5,5-trimethylthiazolidin-4-one was prepared according to the procedure described in Example X by reacting 3.48 g (0.02 m) of 3,5,5-trimethyl-2-oximino thiazolidin-4-one with 3.96 g (0.02 m) of N-methyl-N-(-butylthiosulfenylcarbamoyl fluoride and 1.3 g (0.02 m) of pulverized potassium hydroxide and 0.02 g of crown ether. The residual oil was taken in pentane and chilled to yield 5.0 g of a white solid, m.p. 36°-37° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04232035 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-bb982bd1e24041ffb5fd83ed7f8ddb49 |
| Source note | uspto-grants-1980_11 |