HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 2-Amino-6-(4-fluorophenoxy)benzothiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Benzenamine, 4-(4-fluorophenoxy)- | HCID 147633 | — |
| Reactant | Potassium thiocyanate | HCID 516872 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Amino-6-(4-fluorophenoxy)benzothiazole | HCID 21985512 | 103.2% |
Reaction Steps
A solution of 4-(4′-fluorophenoxy)aniline (0.305 g, 1.50 mmol) and KSCN (0.29 g, 3.00 mmol, 2.0 eq) in 3 mL acetic acid was cooled at about 5° C., and was treated dropwise with a solution of bromine (0.077 mL, 1.50 mmol, 1.0 eq) in 2 mL acetic acid. The mixture was stirred at room temperature for about 2 hours. The precipitate was filtered off and washed with Et2O. The mother liquid from the filtration was concentrated, and the residue was combined with the precipitate. The obtained solid was neutralized with saturated sodium carbonate solution, and a new precipitate was formed. It was filtered off, washed with water, and dried under vacuum to give the desired compound 0.403 g (90%). LC/MS 261.2 (M+1); LC retention time 2.44 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07091227B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-39cabe140ee74440b053a8e259355b3d |
| Source note | uspto-grants-2006_08 |