HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(6-Bromonaphth-2-ylthio)-2-trifluoromethylbenzonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Fluoro-2-(trifluoromethyl)benzonitrile | HCID 605085 | — |
| Reactant | 6-Bromonaphthalene-2-thiol | HCID 19764817 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(6-Bromonaphth-2-ylthio)-2-trifluoromethylbenzonitrile | HCID 17915791 | — |
Reaction Steps
A mixture of 6-bromonaphthalene-2-thiol (956 mg) and 4-fluoro-2-trifluoromethyl benzonitrile (756 mg) in dimethylformamide (15 ml), at ambient temperature, was treated dropwise with triethylamine (504 mg). After stirring at ambient temperature for 3 hours the reaction mixture was diluted with ethyl acetate (100 ml), washed with water (3×25 ml) and brine (25 ml), dried (MgSO4) and evaporated to give a yellow oil. Crystallisation from methanol (20 ml) gave 4-(6-bromonaphth-2-ylthio)-2-trifluoromethylbenzonitrile (1.176 g, mp 114-116° C.;
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173025B1 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-b672429898944e23b01a2d853ad34746 |
| Source note | uspto-grants-2007_02 |