HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 4-(2-bromo-acetyl)-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Acetyl-n-(thiazol-2-yl)benzenesulfonamide | HCID 21082529 | — |
| Reactant | Pyridiniumtribromide | HCID 21124087 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-(2-bromo-acetyl)-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide | HCID 86611697 | — |
Reaction Steps
To a solution of 4-acetyl-N-thiazol-2-yl-benzenesulfonamide (10 mmol) in THF (50 mL) was added pyridinium tribromide (10 mmol), and the mixture was stirred for 4 h. The reaction mixture was diluted with water (30 mL) and the resulting mixture was extracted with ethyl acetate. The organic phase was washed with brine, dried over MgSO4, and concentrated in vacuo. The crude product was purified by column chromatography to give 4-(2-bromo-acetyl)-N-methoxymethyl-N-thiazol-2-yl-benzenesulfonamide (8.2 mmol) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08063080B2 |
| Source dataset | uspto-grants-2011_11 |
| ORD ID | ord-91b89a7ba15f48be93fa5a71156d8de9 |
| Source note | uspto-grants-2011_11 |