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CAS No. : | 1226-42-2 | MDL No. : | MFCD00008405 |
Formula : | C16H14O4 | Boiling Point : | - |
Linear Structure Formula : | CH3OC6H4C(O)C(O)C6H4OCH3 | InChI Key : | YNANGXWUZWWFKX-UHFFFAOYSA-N |
M.W : | 270.28 | Pubchem ID : | 71043 |
Synonyms : |
p-Anisil
|
Chemical Name : | 1,2-Bis(4-methoxyphenyl)ethane-1,2-dione |
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 |
---|---|---|
90% | With potassium hydroxide; In ethanol; at 70℃; for 3h;Inert atmosphere; | (2) Intermediate product 2 (3.69 g, 10 mmol), 4,4'-dimethoxyphenol ester (Compound 3) (2.7 g, 10 mmol) and potassium hydroxide (0.168 g, 3 mmol) were added to the reaction flask, pumped three times, and solvent ethanol (30mL) was injected under nitrogen protection. The resulting mixture was refluxed at 70 C for three hours. After completion of the reaction, the reaction flask was cooled in an ice bath and precipitated to obtain the product. The product was washed with cold ethanol and dried to give red powder product 4 (compound 4). Yield 90%. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
80% | In ethanol; water;Reflux; | Step 2. 2,3-Bis-(4-methoxyphenyl)quinoxaline-6-sulfonic acid A solution of 1,2-bis(4-methoxyphenyl)ethane-1,2-dione (400 mg, 1.48 mmol, 1.00 equiv) and <strong>[7474-78-4]3,4-diaminobenzenesulfonic acid</strong> (278 mg, 1.48 mmol, 1.00 equiv) in ethanol/water (1:1, 20 mL) was stirred overnight at reflux in an oil bath. The resulting mixture was concentrated in vacuo, resulting in 500 mg (80percent) of 2,3-bis-(4-methoxyphenyl)quinoxaline-6-sulfonic acid as a brown solid. |
80% | In ethanol; water;Reflux; | A solution of 1,2-bis(4-methoxyphenyl)ethane-1,2-dione (400 mg, 1.48 mmol, 1.00 equiv) and <strong>[7474-78-4]3,4-diaminobenzenesulfonic acid</strong> (278 mg, 1.48 mmol, 1.00 equiv) in ethanol/water (10/10 mL) was stirred overnight at reflux in an oil bath. The resulting mixture was concentrated under vacuum, yielding 500 mg (80percent) of 2,3-bis(4-methoxyphenyl)quinoxaline-6-sulfonic acid as a brown solid. |