HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → 1,3-Benzenediol, 5-(2-benzothiazolyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | 3,5-Dihydroxybenzaldehyde | HCID 94365 | — |
| Reactant | Sodium Acetate | HCID 517045 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 1,3-Benzenediol, 5-(2-benzothiazolyl)- | HCID 68279367 | 48.8% |
Reaction Steps
An acetic acid (0.8 mL) and sodium acetate (196.6 mg, 2.40 mmol) were added to a suspension including 3,5-dihydroxybenzaldehyde (91.6 mg, 0.66 mmol) and 2-aminothiophenol (0.095 mL, 0.80 mmol, purity: 90%), and then, the reaction mixture was refluxed for 2 hours. The resultant precipitate was filtered, and the filtered product was washed with water and methylene chloride to obtain a gray solid Compound 21 (78.3 mg, 48.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09155690B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-01b3707a449c4a4c86cfd537363abc72 |
| Source note | uspto-grants-2015_10 |