HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl oxamate → ethyl 2-oxo-2H-1,3,4-oxathiazole-5-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl oxamate | HCID 69238 | — |
| Reactant | (Chlorothio)formyl chloride | HCID 75990 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | ethyl 2-oxo-2H-1,3,4-oxathiazole-5-carboxylate | HCID 12351252 | 64.2% |
Reaction Steps
A mixture of 99.7 g (0.85 mol) of ethyl oxamate and 552 g (4.23 mol) of chlorocarbonylsulfenyl chloride, prepared in accordance with British Pat. No. 1,079,348, in toluene was held at reflux for 5.25 hours and then was concentrated under vacuum. Benzene was added to the residue, and the solution was extracted twice with water, twice with 5% NaHCO3, again with water, and was dried (CaSO4) and concentrated under vacuum. The residual oil was filtered to remove sulfur and was crystallized twice from methylcyclohexane to give 95.61 g (64%) of white solid, mp 49°-50.5 C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04115095 |
| Source dataset | uspto-grants-1978_09 |
| ORD ID | ord-0528291c5d4b466f9304b7d585583c65 |
| Source note | uspto-grants-1978_09 |