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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1382482Generated: October 27, 2026

Sulfamic Acid → Acesulfame

https://huagongshe.com/reaction/1382482

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSulfamic AcidHCID 5987—
ReactantAcetoacetamideHCID 80077—
ProductAcesulfameHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04806639
Source datasetuspto-grants-1989_02
ORD IDord-06eb62bfe8cd4f54ab4ecd2a83543fb1
Source noteuspto-grants-1989_02