| Identification | Back Directory | [Name]
4-fluoro-2-(2H-1,2,3-triazol-2-yl)benzoic acid | [CAS]
1293284-50-0 | [Synonyms]
4-fluoro-2-(2H-1,2,3-triazol-2-yl)benzoic acid Benzoic acid, 4-fluoro-2-(2H-1,2,3-triazol-2-yl)- | [Molecular Formula]
C9H6FN3O2 | [MDL Number]
MFCD24481544 | [MOL File]
1293284-50-0.mol | [Molecular Weight]
207.16 |
| Hazard Information | Back Directory | [Synthesis]
To a mixture of 2-bromo-4-fluorobenzoic acid (30 g, 137 mmol), cesium carbonate (89.26 g, 274 mmol), and cuprous iodide (5.27 g, 27.4 mmol) in N,N-dimethylformamide (200 mL) was added N,N'-dimethylcyclohexane-1,2-diamine (3.7 mL, 23.3 mmol) and 1H-1 ,2,3-triazole (18.92 g, 274 mmol). The reaction mixture was stirred at 110 °C overnight, cooled, concentrated under reduced pressure and diluted with deionized water (150 mL). The mixture diluted with water was extracted with ethyl acetate (300 mL × 3). The aqueous layer was acidified with 2N hydrochloric acid and extracted again with ethyl acetate (300 mL × 4). All organic layers were combined, washed with saturated saline (150 mL × 3), dried over anhydrous sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: petroleum ether/ethyl acetate = 100:1 to 5:1) to afford 4-fluoro-2-(2H-1,2,3-triazol-2-yl)benzoic acid (18.13 g) as a yellow solid. Low resolution mass spectrometry (LRMS) showed m/z (M + H)+ of 208.0, which is consistent with the theoretical value of 208.0. | [References]
[1] Patent: WO2015/18027, 2015, A1. Location in patent: Page/Page column 48; 49 [2] Patent: WO2015/18029, 2015, A1. Location in patent: Page/Page column 34; 35 [3] Patent: WO2015/20930, 2015, A1. Location in patent: Page/Page column 40 [4] Patent: WO2016/100157, 2016, A2. Location in patent: Paragraph 36; 37 [5] Patent: WO2016/100162, 2016, A2. Location in patent: Page/Page column 31 |
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