HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → 4-(2-fluoro-4-nitrophenyl)tetrahydro-2-(2-propenyl)-2H-1,2-thiazine 1,1-dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Fluoro-4-nitrophenyl)tetrahydro-2H-1,2-thiazine 1,1-dioxide | HCID 18369148 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-(2-fluoro-4-nitrophenyl)tetrahydro-2-(2-propenyl)-2H-1,2-thiazine 1,1-dioxide | HCID 18369147 | — |
Reaction Steps
Anhydrous potassium carbonate (3.6 g, 26.1 mmol) is added to a solution of 4-(2-fluoro-4-nitrophenyl)tetrahydro-2 H-1,2-thiazine 1,1-dioxide (1.795 g, 6.54 mmol) and allyl bromide (2.0 ml, 23.1 mmol) in dry acetonitrile (25 ml). The mixture is heated to reflux for 5 min then cooled. After filtration and evaporation the residue is chromatographed over silica gel (150 g) eluting with 0-1% methanol-chloroform. The title compound is obtained as flakes (1.70 g, 83%) mp 121°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06348459B1 |
| Source dataset | uspto-grants-2002_02 |
| ORD ID | ord-efc8630e710b4ff19966a532137534f6 |
| Source note | uspto-grants-2002_02 |