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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 127639Generated: October 29, 2026

Carbon Tetrachloride → 2-{2'-[(Morpholinomethyleneamino)sulfonyl]-benzoyl}-1,2-benzoisothiazolin-3-one-1,1-dioxide

https://huagongshe.com/reaction/127639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantPhosgeneHCID 6371—
ReactantN-FormylmorpholineHCID 20417—
ReactantBenzosulfinide sodium; Garantose sodiumHCID 24181110—
SolventDichloromethaneHCID 6344—
Product2-{2'-[(Morpholinomethyleneamino)sulfonyl]-benzoyl}-1,2-benzoisothiazolin-3-one-1,1-dioxideHCID 8673759973.4%

Reaction Conditions

Temperature-30 °C

Reaction Steps

N-formylmorpholine (3 ml) and 2.05 g of anhydrous sodium saccharin were added to 10 ml of dichloromethane. The mixture was cooled to -30° C., and with stirring, 1.65 ml (corresponding to about 5 millimoles of phosgene) of a carbon tetrachloride solution containing 30% of phosgene (W/V %) was added. The temperature of the mixture was raised to room temperature over a period of about 1 hour and stirred at room temperature for 2 hours. The solvent was distilled off under reduced pressure. Water was added to the remaining oily product, and under ice cooling, the mixture was stirred until the oily product crystallized. The crystals were collected by filtration, thoroughly washed with water, and dried to afford 1.70 g of white crystals (yield 73.4%), decomposition point:160°-169° C. Recrystallization of the crude crystals from acetone yielded white needle-like crystals having a decomposition point of 173° to 175° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04256744
Source datasetuspto-grants-1981_03
ORD IDord-76907ab5b41a4fe0b73925e7ce9bf962
Source noteuspto-grants-1981_03