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CAS No. : | 130336-16-2 | MDL No. : | MFCD01319996 |
Formula : | C8H3Cl2F3O | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | DZDSQRPDUCSOQV-UHFFFAOYSA-N |
M.W : | 243.01 | Pubchem ID : | 2758231 |
Synonyms : |
|
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | H302-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 |
---|---|---|
40% | Lithium diisopropylamide (Aldrich Chemical Company, 2M in tetrahydrofuran/ ethylbenzene, 4 mL, 7.94 mmol) was added to tetrahydrofuran (4 mL) at -78 0C. A solution of l-(4-bromo-l-naphthalenyl)ethanone (1.8 g, 7.22 mmol) in tetrahydrofuran (4 mL) was added dropwise to the mixture. When the addition was complete the mixture was stirred for 30 min at -78 0C. Then a solution of l-(3,5-dichlorophenyl)-2,2,2-trifluoroethanone (1.75 g, 7.20 mmol) in tetrahydrofuran (4 mL) was added dropwise to the mixture at such a rate that the temperature of the reaction mixture did not exceed -55 0C. The mixture was allowed to warm to ambient temperature over 120 min. The mixture was then poured into IN hydrochloric acid (100 mL) and extracted with ethyl acetate (2 x 100 mL). The combined extracts were dried and evaporated. Chromatography on silica gel (eluted with 1 :9 ethyl acetate/ hexanes) and crystallization from hexanes gave the title product as a white solid (1.1 g, 40% yield) melting at 74.5-75 0C (after recrystallization from hexanes). IR (nujol) 3409, 1684, 1569, 1505, 1407, 1343, 1232, 1170, 1141, 1121 cm-1.1H NMR (CDCl3) delta 8.38-8.30 (m, 2H), 7.90 (d, J=7.7 Hz, IH), 7.73-7.61 (m, 3H), 7.52 (s, 2H), 7.36 (t, J=I.8 Hz, IH), 5.86 (s, IH), 3.87 (1/2ABq, J=17.1 Hz, IH), 3.80 (1/2ABq, J=IlA Hz, IH). |
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