HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 4-Bromo-1,3-benzothiazol-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Benzothiazol-5-amine | HCID 70749 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-1,3-benzothiazol-5-amine | HCID 22462223 | 86.6% |
Reaction Steps
A stirred solution of 3 g of 5-aminobenzothiazole in 100 ml of acetonitrile at room temperature was treated with 3.5 g of N-bromosuccinimide and the resulting solution was stirred at room temperature for 4 hours. The solvent was removed under reduced pressure and the residue purified by silica gel chromatography (eluent cyclohexane/ethyl acetate 7:3) to afford 3.9 g of 5-amino-4-bromobenzothiazole as a pink solid. MS (ES+) 229/231 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08338443B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-acd3c265866944a19ce987aa0fab50dc |
| Source note | uspto-grants-2012_12 |