HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sulfamic Acid → Acesulfame
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | Acetoacetamide | HCID 80077 | — |
| Product | Acesulfame | HCID 36573 | — |
Reaction Steps
cyclizing the acetoacetamide derivative; the process comprises using, as the sulfamic acid derivative in stage (a), a salt of sulfamic acid which is at least partly soluble in the inert organic solvent employed, cyclizing the acetoacetamide-N-sulfonate formed in this stage or the free acetoacetamide-N-sulfonic acid in stage (b) by the action of an at least approximately equimolar amount of SO3, if appropriate in an inert inorganic or organic solvent, to give 6-methyl-3,4-dihydro-1,2,3-oxathiazin-4-one 2,2-dioxide, and then, if desired, also neutralizing with a base, in a stage (c), the product obtained here in the acid form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04806639 |
| Source dataset | uspto-grants-1989_02 |
| ORD ID | ord-06eb62bfe8cd4f54ab4ecd2a83543fb1 |
| Source note | uspto-grants-1989_02 |