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| | 3-Cyano-4-fluorobenzyl bromide Basic information |
| Product Name: | 3-Cyano-4-fluorobenzyl bromide | | Synonyms: | 3-Cyano-4-fluorobenzyl bromide, alpha-Bromo-6-fluoro-m-tolunitrile;Benzonitrile, 5-(bromomethyl)-2-fluoro-;3-cyano-4-fluorobromobenzyl;5-(BroMoMethyl)-2-fluorobenzonitrile;3-Cyano-4-fluorobenzyl bromide | | CAS: | 180302-35-6 | | MF: | C8H5BrFN | | MW: | 214.03 | | EINECS: | | | Product Categories: | Fluorine series | | Mol File: | Mol File |  |
| | 3-Cyano-4-fluorobenzyl bromide Chemical Properties |
| Boiling point | 272.7±25.0 °C(Predicted) | | density | 1.59±0.1 g/cm3(Predicted) | | storage temp. | Storage temp. 2-8°C | | form | fused solid | | color | White to off-white to faint yellow | | Sensitive | Lachrymatory |
| Hazard Codes | C,Xn | | Risk Statements | 22 | | Hazard Note | Corrosive/Lachrymatory | | HS Code | 2926907090 |
| | 3-Cyano-4-fluorobenzyl bromide Usage And Synthesis |
| Uses | 3-CYANO-4-FLUOROBENZYL BROMIDE is used in the synthetic preparations of thrombin inhibitors. | | Synthesis | General procedure for the synthesis of 2-fluoro-5-(bromomethyl)benzonitrile from 2-fluoro-5-methylbenzonitrile: 2-fluoro-5-methylbenzonitrile (3.00 g, 22 mmol), N-bromosuccinimide (4.12 g, 23 mmol), and benzoyl peroxide (1.07 g, 4.4 mmol) were dissolved in carbon tetrachloride (100 mL) and heated to reflux for 6 hours. Upon completion of the reaction, the mixture was cooled to room temperature and subsequently mixed with water. The organic phase was separated, dried with anhydrous magnesium sulfate and filtered through diatomaceous earth (Celite). The filtrate was concentrated under reduced pressure and purified by fast column chromatography (n-hexane/ethyl acetate, 20:1) to afford 5-(bromomethyl)-2-fluorobenzonitrile (1.58 g, 33% yield) as an oil.1H NMR (CDCl3, 400 MHz) data were as follows: δ 4.45 (s, 2H), 7.21 (m, 1H), 7.65 (m, 2H). | | References | [1] Journal of Medicinal Chemistry, 2016, vol. 59, # 20, p. 9422 - 9430
[2] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 20, p. 2925 - 2930
[3] Helvetica Chimica Acta, 2017, vol. 100, # 12,
[4] Patent: WO2010/93845, 2010, A1. Location in patent: Page/Page column 86
[5] Bioorganic and Medicinal Chemistry Letters, 1998, vol. 8, # 7, p. 715 - 720 |
| | 3-Cyano-4-fluorobenzyl bromide Preparation Products And Raw materials |
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