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CAS No. : | 52771-21-8 | MDL No. : | MFCD00042406 |
Formula : | C8H5F3O2 | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | FQEVHRCPXFKJHF-UHFFFAOYSA-N |
M.W : | 190.12 | Pubchem ID : | 605139 |
Synonyms : |
|
Signal Word: | Warning | Class: | |
Precautionary Statements: | P305+P351+P338 | UN#: | |
Hazard Statements: | H227-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 |
---|---|---|
71% | With sodium hydrogensulfite; In N,N-dimethyl acetamide; at 150℃; | General procedure: Sodium hydrogen sulfite (4 mmol) was added to a solution of anthranilamide 1 (2 mmol) and benzaldehyde 2 (2 mmol) in N,N- dimethylacetamide (5 mL). The mixture was heated under continuous stirring at 150 o C for 2-3 h and poured into ice water. The precipitate was then filtered, washed with water followed byethanol, and dried to yield the 2-arylquinazolinones 3-31.#10;#10; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
98% | With hydrogen; In methanol; at 20℃; for 5h; | General procedure: A mixture of 1a (196 mg, 1 mmol) and 1%Pd/Ni bimetallic catalyst9 (60 mg, 30 wt %) in MeOH (10 mL) was stirred underH2 at room temperature and atmospheric pressure (on an atmosphericpressure hydrogenation apparatus) until the absorption of hydrogen ceased(3.5 h). After the catalyst was removed off by a magnetic stirring bar, thesolution was evaporated in a vaporator to give the product 2a |
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