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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1917238Generated: November 2, 2026

Sodium Iodide → 2,3-Dihydro-1,4-benzothiazine

https://huagongshe.com/reaction/1917238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-(2-Chloroethylthio)anilineHCID 12761371—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product2,3-Dihydro-1,4-benzothiazineHCID 15106499%

Reaction Conditions

Temperature90 °C

Reaction Steps

To a stirred solution of 2-(2-chloroethylthio)aniline (850 mg, 4.53 mmol) in DMF (10 mL) was added potassium carbonate (1878 mg, 13.59 mmol) followed by sodium iodide (67.9 mg, 0.453 mmol). The resulting mixture was heated to 90° C. and stirred overnight. The reaction mixture was then cooled to room temperature, diluted with ethyl acetate, and washed with water (3×) and brine. The organic phase was dried, filtered, concentrated, and then chromatographed in 9:1 hexanes:ethyl acetate, giving an orange oil (675 mg, 99%). 1H NMR (DMSO-d6) δ 6.85-6.75 (m, 2H), 6.51-6.39 (m, 2H), 6.00 (brs, 1H), 3.49-3.44 (m, 2H), 2.98-2.93 (m, 2H); ESI-MS (m/z, %): 152 (MH+, 100), 124 (44).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618286B2
Source datasetuspto-grants-2013_12
ORD IDord-24112c0034164af698a2dcd5b8551f49
Source noteuspto-grants-2013_12