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CAS No. : | 849758-12-9 | MDL No. : | MFCD08436044 |
Formula : | C8H6BrFO2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | WDAFDKXHLVMFKA-UHFFFAOYSA-N |
M.W : | 233.03 | Pubchem ID : | 21951878 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P301+P312-P302+P352-P304+P340-P305+P351+P338 | UN#: | |
Hazard Statements: | H302-H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
* 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 |
---|---|---|
92% | With diisobutylaluminium hydride; In tetrahydrofuran; at 20℃; | To a solution of 4-bromo-3-fluoro-benzoic acid methyl ester (5.3 g, 22.9 mmol) in dry THF (60 mL) was added diisobutylaluminum hydride (30 mL) dropwise, This mixture was stirred overnight at room temperature until the starting material had been consumed, quenched with saturated aqueous potassium tartrate solution and extracted with ethyl acetate (3×50 mL). The combined organic layer was washed with brine, dried with Na2SO4, filtered, and evaporated to give white solid product (4.3 g, 92%). |
A cooled (0 0C) suspension of lithium aluminum hydride (88 mg; 2.3 mmol) in anhydrous THF (10 mL) was treated dropwise with a solution of methyl 4-bromo-3-fluorobenzoate (Combi-Blocks; 300 mg; 1.29 mmol) dissolved in anhydrous Et2O (10 mL), and the reaction mixture was stirred at RT for 2 days. The reaction mixture was treated with a saturated aqueous solution of sodium thiosulfate. The organic phase was separated, dried over MgSO4, filtered and concentrated to dryness affording the title compound as a yellow liquid (247 mg, 94%). 1H NMR (300MHz, DMSO-d6) delta [ppm] 7.64 (1 H, dd, J= 8.1 , J= 7.5 Hz), 7.28 (1 H, m), 7.11 (1 H, m), 5.40 (1 H, t, J= 5.8 Hz), 4.48 (2H, d, J= 5.8 Hz). HPLC (Condition A): Rt 2.78 min (HPLC purity 90.2%). |
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