HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Aminothiophenol → 2-(2-Aminophenyl)sulfanylbenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Aminothiophenol | HCID 8713 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chlorobenzonitrile | HCID 13391 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(2-Aminophenyl)sulfanylbenzonitrile | HCID 366233 | 84.5% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
In 10 ml of DMF was dissolved 1.25 g of orthoaminothiophenol followed by addition of 1.38 g of potassium carbonate. The mixture was preheated at 100° C. and after 1.45 g of o-chlorobenzonitrile was added, the mixture was stirred in an argon gas stream at 100° C. for 1 hour. To the reaction mixture was added ice-water and the mixture was extracted with ethyl acetate. The extract was washed with water twice and dried over magnesium sulfate and the solvent was distilled off. The residue was crystallized from n-hexane-isopropyl ether to give 1.91 g of the title compound as white crystals, m.p. 88°-90° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05399703 |
| Source dataset | uspto-grants-1995_03 |
| ORD ID | ord-e4752e23f9ad422380fae808ae1345c7 |
| Source note | uspto-grants-1995_03 |