HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 2-Amino-5-bromobenzene-1-thiol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | 2-Benzothiazolamine, 6-bromo- | HCID 85149 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-5-bromobenzene-1-thiol | HCID 1209045 | 63.2% |
Reaction Steps
Potassium hydroxide (39.6 g) was dissolved at 0° C. in water (80 mL), and 2-amino-6-bromobenzothiazole (6.87 g) was added to the solution, followed by refluxing under heating overnight. The mixture was returned to room temperature, and then neutralized with 5N aqueous acetic acid solution. The precipitated crystals were recovered through filtration, washed with water, and dried under reduced pressure with heating, followed by recrystallization from isopropyl ether, to thereby yield the title compound (3.87 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022075B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-95dfb255a5eb49f497aad75ae6f1451b |
| Source note | uspto-grants-2011_09 |