HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → HCID 19969463, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Fluoro-5-nitrobenzonitrile | HCID 519417 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 19969463 | HCID 19969463 | — |
Reaction Steps
2-Aminothiophenol (6.26 g, 50 mmol) was added to a mixture of sodium hydride (2.0 g of 60% oil dispersion, 50 mmol) in DMF (100 ml) at 0° under nitrogen. After stirring for 30 minutes at 0°, 2-fluoro-5-nitrobenzonitrile (8.3 g, 50 mmol) in DMF (20 ml) was added and the mixture kept at room temperature overnight. The reaction mixture was evaporated and azeotroped with toluene, then the residue was partitioned between chloroform and water and the layers separated. Drying (sodium sulphate) and evaporation of the organic layer gave a residue which was separated from chloroform as bright yellow crystals (10.1 g, Rf 0.52 in 1:1 ethyl acetate/hexane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05607929 |
| Source dataset | uspto-grants-1997_03 |
| ORD ID | ord-261cc5b59d4b4cfcb1d41aa11b6cc69b |
| Source note | uspto-grants-1997_03 |