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CAS No. : | 2051-90-3 | MDL No. : | MFCD00000811 |
Formula : | C13H10Cl2 | Boiling Point : | No data available |
Linear Structure Formula : | (C6H5)CCl2(C6H5) | InChI Key : | - |
M.W : | 237.12 | Pubchem ID : | - |
Synonyms : |
|
Signal Word: | Danger | Class: | 8 |
Precautionary Statements: | P260-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338 | UN#: | 3265 |
Hazard Statements: | H314-H335 | Packing Group: | Ⅱ |
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 |
---|---|---|
76% | at 160℃; for 0.666667h; | A suspension of the corresponding methyl 2,3-dihydroxybenzoate (1 eq.) in dichlorodiphenylmethane (1.5 eq.) was stirred at 160 C. for 40 min. After cooling to 50 C., 30 mL MeOH was added to the viscous brown oil leading to the formation of a precipitate. The precipitate was filtered, washed with MeOH (3×20 mL) and dried under high vacuum to yield the desired compound as a colorless solid. ; <strong>[105603-49-4]Methyl 5-bromo-2,3-dihydroxybenzoate</strong> (3 g, 12.87 mmol, 1 eq.) was reacted with dichlorodiphenylmethane (3.7 mL, 4.58 g, 19.31 mmol, 1.5 eq.) according to GP2, Method A. Yield: 4 g (76%). Colorless powder. Mp.: 146-148 C. IR (KBr): 3079w, 2950w, 1718s (CO); 1467s; 1355s; 1238s; 1204s; 1043s; 1013s; 944m; 867m; 780s. 1H-NMR (300 MHz, CDCl3); 3.94 (s, 3 H, CH3); 7.14 (d, J=1.9, 1 H, Harom, Cat.); 7.38-7.41 (m, 6 H, Harom, Ketal); 7.55-7.59 (m, 5 H, Harom, Cat., Harom, Ketal). 13C-NMR (75 MHz, CDCl3): 52.4; 112.6; 113.7; 115.6; 119.1; 125.0; 126.2; 128.3; 129.4; 139.0; 147.5; 149.1; 163.7. HR-MS (MALDI): calcd. for C21H16BrO4 ([M+H]+): 411.0231, found 411.0220. |
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