HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dibromoethane → 2,3-Dihydro-1,4-benzothiazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dibromoethane | HCID 7839 | — |
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2,3-Dihydro-1,4-benzothiazine | HCID 151064 | 66.1% |
Reaction Steps
K2CO3 (4.4 g, 31.9 mmol) and 1,2-dibromoethane (0.69 mL, 8.0 mmol) were added to a solution of 2-aminothiophenol (1.0 g, 8.0 mmol) in 20 mL of acetone at room temperature. The reaction mixture was stirred overnight. The insoluble material was filtered off and the solvent was removed under reduced pressure. The residue was purified on silica gel column to provide 3,4-dihydro-2H-1,4-benzothiazine (0.8 g, 66%). MS (ES+): 152 (M+1)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06890915B2 |
| Source dataset | uspto-grants-2005_05 |
| ORD ID | ord-cc4a33992b1846e687b8eea052032b1e |
| Source note | uspto-grants-2005_05 |