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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1296308Generated: November 2, 2026

Iodine → HCID 86597542, compound

https://huagongshe.com/reaction/1296308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIodineHCID 807—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 68690328HCID 68690328—
SolventDichloromethaneHCID 6344—
ProductHCID 86597542HCID 86597542—

Reaction Steps

To a solution of 2-(2-propenyl)-5-trifluoromethylbenzenesulfonamide (780 mg, 2.94 mmol) in nitrogen-degassed dichloromethane (30 mL) containing potassium carbonate (1.62 g, 11.8 mmol) was added iodine (1.49 g, 5.88 mmol). After stirring for 2 h, the reaction was quenched with 10% aqueous sodium thiosulfate (ca. 14 mL). The dichloromethane was removed in vacuo and the residue was diluted with methanol (10 mL) and 0.25 N potassium carbonate in 70% aqueous methanol. Additional methanol was added to produce a nearly homogeneous solution. After 10 min, the reaction was concentrated in vacuo to remove most of the methanol. The residue was partitioned between dichloromethane (30 mL) and water (10 mL). The aqueous layer was extracted with dichloromethane (5 mL) and the combined organic layers were dried (magnesium sulfate) and concentrated in vacuo to provide 8,8a-dihydro-5-(trifluoromethyl)-1H-azirino[1,2-b][1,2]benzothiazine 3,3-dioxide as a white solid (685 mg (92%): LCMS (net. ion spectrum) m/z 262.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07244843B2
Source datasetuspto-grants-2007_07
ORD IDord-e288b1176b70488caa6401c26119c233
Source noteuspto-grants-2007_07