HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 55589-62-3
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Sulfuryl fluoride | HCID 17607 | — |
| Reactant | Acetoacetamide | HCID 80077 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 55589-62-3 | HCID 23683747 | 48.2% |
Reaction Steps
10.1 g (0.1 mol) of acetoacetamide, 50.5 g (0.5 mol) of triethylamine and 100 ml of acetonitrile were introduced into a round-bottomed flask fitted with a stirrer and a solid carbon dioxide condenser, as in Example 1. 15.3 g (0.15 mol) of sulfuryl fluoride gas were passed in over a period of 20 minutes. The reaction mixture was then allowed to warm up to room temperature, with stirring. After stirring for 2 hours, 230 ml (0.46 mol) of 2N methanolic KOH were added dropwise and the product was filtered off with suction. 9.7 g (48% of theory) of Acesulfam K were obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04625024 |
| Source dataset | uspto-grants-1986_11 |
| ORD ID | ord-f531db0df2e64c5fbe6e6ae4a65f2dd7 |
| Source note | uspto-grants-1986_11 |