HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → Amino-2-[2-(4-cyanophenyl)ethylthio]benzene
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 22033501 | HCID 22033501 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Amino-2-[2-(4-cyanophenyl)ethylthio]benzene | HCID 22033547 | 82.4% |
Reaction Steps
4-Toluenesulfonic acid, 2-(4-cyanophenyl)ethyl ester (1.9 g; 6.3 mmol; from Example 18(i) above) and K2CO3 (2.0 g) were added to a solution of 2-aminothiophenol (0.875 g; 7.0 mmol) in EtOH (20 mL). The mixture was heated to reflux for 48 hours, cooled, filtered and concentrated in vacuo to an oil which was dissolved in EtOAc (50 mL) and washed with water (25 mL). The organic portion was dried (MgSO4) and concentrated. The residue was purified by flash chromatography (SiO2; Et2O:hexane (1:1)) to obtain 1.32 g (78%) of the sub-title product as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06221898B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-33ffd13a03974ccc9cd55a3d7d722357 |
| Source note | uspto-grants-2001_04 |