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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 424586Generated: October 29, 2026

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

https://huagongshe.com/reaction/424586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 12761371HCID 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 numberUS08106043B2
Source datasetuspto-grants-2012_01
ORD IDord-149cb4f121e84d469e927e3479021c6a
Source noteuspto-grants-2012_01