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CAS No. : | 930599-57-8 | MDL No. : | MFCD27933385 |
Formula : | C8H6F3I | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | VVIDIHOUJXGOHT-UHFFFAOYSA-N |
M.W : | 286.03 | Pubchem ID : | 58016746 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H315-H319-H335 | Packing Group: | N/A |
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 |
---|---|---|
85% | To intennediate 164c (6.0 g, 34,26 mmol, 1 .00 equiv) in water (50 mL) at 0 C was added sulfuric acid (7.06 g, 71.98 mmol, 2.10 equiv) followed by the drop-wise addition of a solution of NaN02 (2.60 g, 37.68 mmol, 1.10 equiv) in water (40 mL) and the mixture was stirred for 1 h. To this was added drop-wise a solution of KI (7.97 g, 48.01 mmol, 1.40 equiv) in water (40 mL) and the reaction was allowed to warm to RT and stirred for 1 h. The mixture was diluted with 200 ml, of ethyl acetate, washed with 2 x 200 ml. of Brine, 1 x 200 mL of aqueous Na^SOa , dried over anhydrous sodium sulfate and concentrated. The residue was purified via silica, gel chromatography (petroleum ether/ethyl acetate, 100:1) to afford 8.2 g (85%) of intermediate 164d as a yellow oil. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
36% | With N-Bromosuccinimide; dibenzoyl peroxide; In tetrachloromethane; at 60℃; | To intermediate 164d (3.5 g, 12.24 mmol, 1.00 equiv) in CC14 (40 mL) at 60 C was added benzoyl peroxide (1.7 g, 7.02 mmol, 0.57 equiv) followed by the batch-wise addition of NBS (2.37 g, 13.32 mmol, 1.09 equiv) and the reaction stirred at reflux overnight. The solids were filtered out and the filtrate concentrated to afford 1.6 g (36%) of intermediate 164e as a red oil. |
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