HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → Benzo(d)thiazol-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Thiocyanate | HCID 9322 | — |
| Reactant | Diphenylamine | HCID 11487 | — |
| Reactant | Bromine | HCID 24408 | — |
| Product | Benzo(d)thiazol-2-amine | HCID 8706 | — |
Reaction Steps
If the desired 2-amino benzenethiol 14-scheme 12 is not commercially available it can be synthesized by reaction of the phenyl aniline with the thiocyanate anion in the presence of an oxidant (like bromine) to produce the 2-amino benzthiazole. This thiazole can then be hydrolyzed to the desired 2-amino benzenethiol 12-scheme 10 with a strong base like NaOH in a protic solvent (i.e., EtOH).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06133319 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-7790a7772dc343f882de697649dadc6f |
| Source note | uspto-grants-2000_10 |