HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 6-bromo-3,4-dihydro-1H-2lambda6,1-benzothiazine-2,2-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 3192-06-1 | HCID 12203335 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-bromo-3,4-dihydro-1H-2lambda6,1-benzothiazine-2,2-dione | HCID 69108075 | 79.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09434761B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-c88953e3d60947be945fb965a6c5a488 |
| Source note | uspto-grants-2016_09 |