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| | 4-Chloro-2-(trifluoromethyl)benzonitrile Basic information | | Application |
| Product Name: | 4-Chloro-2-(trifluoromethyl)benzonitrile | | Synonyms: | 4-chloro-2-(trifluoronethyl)benzonitrile;2-trifluoromethyl-4-chlorophenyl-carbonitrile;2-TRIFLUOROMETHYL-4-CHLOROBENZONITRILE;5-CHLORO-2-CYANOBENZOTRIFLUORIDE;4-CHLORO-2-(TRIFLUOROMETHYL)BENZONITRILE;3-Chloro-6-cyanobenzotrifluoride;5-Chloro-2-cyanobenzotrifluoride 98%;5-Chloro-2-cyanobenzotrifluoride98% | | CAS: | 320-41-2 | | MF: | C8H3ClF3N | | MW: | 205.56 | | EINECS: | | | Product Categories: | Fluorine series;Fluorobenzene | | Mol File: | 320-41-2.mol |  |
| | 4-Chloro-2-(trifluoromethyl)benzonitrile Chemical Properties |
| Hazard Codes | T | | RIDADR | UN3276 | | Hazard Note | Toxic | | HazardClass | 6.1 | | PackingGroup | III | | HS Code | 2926907090 |
| | 4-Chloro-2-(trifluoromethyl)benzonitrile Usage And Synthesis |
| Application | 4-Chloro-2-trifluoromethylbenzonitrile (1) is an important intermediate in the synthesis of bicalutamide. In addition, due to its multiple reaction sites, it is widely used in the preparation of pharmaceutical and chemical intermediates. | | Chemical Properties | Yellow liquid | | Synthesis | General procedure for the synthesis of 2-trifluoromethyl-4-chlorobenzonitrile from 2-iodo-5-chlorobenzotrifluoride and zinc cyanide: 4-chloro-1-iodo-2-trifluoromethylbenzene (1500 mg, 4.89 mmol), zinc cyanide (345 mg, 2.94 mmol) and tetrakis(triphenylphosphine)palladium(0) (564 mg, 0.488 mmol), then N,N-dimethylformamide (40 mL) was added. The reaction mixture was heated at 80 °C for overnight reaction. After the reaction was completed, it was cooled to room temperature, the reaction solution was diluted with toluene, washed sequentially with 2N ammonium hydroxide solution (3 times) and saturated aqueous sodium chloride solution, and the organic phase was filtered after drying and concentrated to obtain the crude product. The crude product was purified by silica gel column chromatography with hexane/dichloromethane as eluent to give 4-chloro-2-trifluoromethylbenzonitrile (630 mg, 63% yield). The structure of the product was confirmed by 1H NMR (400 MHz, CDCl3): δ 7.81-7.78 (m, 2H), 7.67 (dd, 1H, J = 8.4, 2.4 Hz). | | References | [1] Patent: WO2006/44454, 2006, A1. Location in patent: Page/Page column 63 |
| | 4-Chloro-2-(trifluoromethyl)benzonitrile Preparation Products And Raw materials |
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