HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → 4-(4-Benzyloxy-2-nitro-phenylsulfanyl)-phenylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4-Aminothiophenol | HCID 14510 | — |
| Reactant | 5-Benzyloxy-2-chloro-nitrobenzene | HCID 11043622 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Benzyloxy-2-nitro-phenylsulfanyl)-phenylamine | HCID 66808306 | 83% |
Reaction Steps
A solution of the compound prepared in Example 214A (1.0 g, 3.80 mmol), 4-aminothiophenol (0.5 g, 4.00 mmol), cesium carbonate (1.3 g, 4 mmol) in dimethylformamide (10 ml) was heated at 40° C. for 16 hours. Afterwards, ice water (50 mL) was added to the solution and the resultant slurry was treated with ethyl acetate (100 ml). The layers were separated and the organic layer was washed with 10% sodium bicarbonate and 10% sodium chloride, then dried over anhydrous sodium sulfate. The drying agent was filtered and solvent was removed under vacuum leaving an orange oil as the title compound, (1.1 g, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07915411B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-ed2e7b96c85f4c33b00c948e44bd6bca |
| Source note | uspto-grants-2011_03 |