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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 58861Generated: October 30, 2026

Water → 6-bromo-3,4-dihydro-1H-2lambda6,1-benzothiazine-2,2-dione

https://huagongshe.com/reaction/58861

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantN-bromobutanimideHCID 67184—
Reactant3192-06-1HCID 12203335—
SolventDimethylformamideHCID 6228—
Product6-bromo-3,4-dihydro-1H-2lambda6,1-benzothiazine-2,2-dioneHCID 6910807579.1%

Reaction Steps

NBS (1.5 g, 8.2 mmol) was added to a solution of 3,4-dihydro-1H-benzo[c][1,2]thiazine 2,2-dioxide (1.5 g, 8.2 mmol) in DMF (15 mL). The reaction mixture was stirred overnight at ambient temperature followed by addition of water (200 mL) and EtOAc (100 mL). The two layers were separated and the aqueous phase was extracted with EtOAc (100 mL×3). The combined organic phases were washed with brine (200 mL×3), dried over anhydrous sodium sulfate, and concentrated. The residue was purified by flash column chromatography on silica gel (EtOAc/hexane=1:3) to afford 6-bromo-3,4-dihydro-1H-benzo[c][1,2]thiazine 2,2-dioxide (1.7 g, 79% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09434761B2
Source datasetuspto-grants-2016_09
ORD IDord-c88953e3d60947be945fb965a6c5a488
Source noteuspto-grants-2016_09