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CAS No. : | 2267-23-4 | MDL No. : | MFCD00042326 |
Formula : | C7H5F3N2O3 | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | YCGFVAPIBALHRT-UHFFFAOYSA-N |
M.W : | 222.12 | Pubchem ID : | 2775772 |
Synonyms : |
|
Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P261-P280-P305+P351+P338-P311 | UN#: | 2811 |
Hazard Statements: | H302+H312-H315-H319-H331-H335 | Packing Group: | Ⅲ |
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 |
---|---|---|
78% | With tert.-butylnitrite; copper(ll) bromide In acetonitrile at 20℃; for 1 h; | INTERMEDIATE 244-Bromo-3-nitrophenyl trifiuoromethyl ether To a solution of 2-nitro-4-[(trifluoromethyl)oxy]aniline (2.0 g, 9.0 mmol) in acetonitrlle (50 mL) was added tert-butylnitrite (7.4 g, 72 mmol). The solution was stirred 2 min and then Copper(II) bromide (40 g, 180 mmol) was added. The solution stirred for 1 h at rt. The reaction was partitioned between EtOAc (500 mL) and 1N HCl (aq) (100 mL). The layers were separated, and the organics were washed with 1N HCl (aq) (3.x.50 mL), dried over MgSO4, filtered, and the volatiies were evaporated under reduced pressure, and the residue was purified by flash column chromatography (0 to 20percent EtOAc:hexanes) to give 2.0 g (78percent) of the title compound. 1H NMR (400 MHz, CDCl3): δ 7.78 (d, J=8.79 Hz, 1H), 7.76 (s, 1H), 7.32 (s, 1H, J=8.79 Hz). |
78% | With tert.-butylnitrite; copper(ll) bromide In acetonitrile at 20℃; for 1 h; | Intermediate 24: 4-Bromo-3-πitrQphenyi..trjflMQ.romet.h.y.J..etherTo a solution of 2-nitro-4-[(tπ^uoromoethyi)oxy]arsHine (2.0 g, 9.0 mrno.) "m acetoπitrile (50 mL) was added te/.pound.butyinitrite (7.4 g, 72 mmol). The solution was stirred 2 min and then Copper(ll) bromide (40 g, 180 mmol) was added. The solution stirred for 1 h at rt The reaction was partitioned between EtOAc (500 rπL) and 1 N HCi (aq) (100 mL). The iayers were separated, and the organics were washed mth 1N HCi (aq) (3 x 50 ml), dried over .VlgS04, filtered, and the volatiles were evaporated under reduced pressure, and the residue was purified by flash column chromatography (0 to 20percent <n="117"/>EiOAc:hexanes) to give 2,0 g (78percent) of the title compound. 1H NMR (400 MHz, CDCI3): δ 7.78 (ds J- 8.79 Hz, 1H), 7,76 (s, IH), 7,32 (s, 1 H, J- 8.79 Hz). |
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