Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2172829Generated: October 29, 2026

Saccharin → Pseudosaccharin chloride

https://huagongshe.com/reaction/2172829

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSaccharinHCID 5143—
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Solvent1,4-DioxaneHCID 31275—
ProductPseudosaccharin chlorideHCID 64783—

Reaction Conditions

Temperature110 °C

Reaction Steps

To a solution of o-sulfobenzimide (5.00 g) in dioxane (20 ml) were added thionyl chloride (7.5 ml) and dimethylformamide (0.25 ml), and the mixture was stirred overnight at 110° C. The reaction mixture was concentrated under reduced pressure, and to the residue was added toluene (20 ml) to give 3-chloro-1,2-benzisothiazole 1,1-dioxide (3.77 g) as crystals. The obtained 3-chloro-1,2-benzisothiazole 1,1-dioxide (3.77 g) was dissolved in dioxane (20 ml), 3-aminorhodanine (2.77 g) was added thereto, and the mixture was stirred at 110° C. for 1 hr. The reaction mixture was concentrated under reduced pressure, and to the residue was added chloroform (20 ml) to give 3-[(4-oxo-2-thioxothiazolidin-3-yl)amino]-1,2-benzisothiazole 1,1-dioxide (3.56 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056862B2
Source datasetuspto-grants-2015_06
ORD IDord-63ab9d8cedb643ec8b9a5d3812ccacb7
Source noteuspto-grants-2015_06