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CAS No. : | 78239-71-1 | MDL No. : | MFCD09037367 |
Formula : | C7H5Br2F | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | ZRWSODQPUJMFRV-UHFFFAOYSA-N |
M.W : | 267.92 | Pubchem ID : | 12922710 |
Synonyms : |
|
Signal Word: | Danger | Class: | 8 |
Precautionary Statements: | P234-P260-P264-P280-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P390-P405-P406-P501 | UN#: | 3261 |
Hazard Statements: | H290-H314 | Packing Group: | Ⅱ |
GHS Pictogram: |
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* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
75% | In dimethyl sulfoxide; for 18h; | A solution of 2-bromo-4-(bromomethyl)-1 -fluorobenzene (5.0 g, 18.7 mmol) in DMSO (80 ml_) was treated with sodium cyanide (1.16 g, 22.4 mmol) and <n="100"/>stirred for 18 hours. The reaction was poured into ethyl acetate and washed 4x with 5% sodium chloride. The organic layer was dried over magnesium sulfate, filtered, and concentrated to an oil. Purification by silica gel column chromatography provided the title compound as a light amber oil (3.6 g, 75%). LC/MS: 10% - 90% CH3CN:H20 gradient over 5 minutes: 2.57 min. ,214, 216 (M+H); 1H NMR (400 MHz, CHLOROFORM-c/) delta ppm 3.73 (s, 2 H) 7.15 (t, J=8.40 Hz, 1 H) 7.20 - 7.32 (m, 1 H) 7.56 (dd, J=6.25, 2.35 Hz, 1 H). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
88.9% | With tetrabutylammomium bromide; In dichloromethane; water; at 20℃; for 4h; | 2-bromo-4-(bromomethyl)-1-fluorobenzene (20.000 g, 74.649 mmol), potassium cyanide (14.583 g, 223.947 mmol) and tetra-n-butylammonium bromide (2.406 g, 7.465 mmol) was dissolved in a mixed solution of dichloromethane(80 mL)/water (80 mL) at room temperature and stirred at the same temperature for 4 hours. The reaction mixture was poured into water and extracted with dichloromethane. The organic layer was washed with saturated sodium hydrogen carbonate aqueous solution, and water was removed with anhydrous magnesium sulfate, followed by filtration and concentration under reduced pressure. The concentrate was purified and purified by column chromatography (SiO2, 120 g cartridge; ethyl acetate / hexane = 0% to 20%) to give the title compound (14.200 g, 88.9%) as a colorless liquid. |
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