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CAS No. : | 14737-89-4 | MDL No. : | MFCD00004387 |
Formula : | C11H12O4 | Boiling Point : | - |
Linear Structure Formula : | (CH3O)2C6H3CHCHCOOH | InChI Key : | HJBWJAPEBGSQPR-GQCTYLIASA-N |
M.W : | 208.21 | Pubchem ID : | 717531 |
Synonyms : |
|
Chemical Name : | (E)-3-(3,4-Dimethoxyphenyl)acrylic acid |
Signal Word: | Warning | Class: | N/A |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | N/A |
Hazard Statements: | 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 |
---|---|---|
83% | With lithium aluminium tetrahydride; In tetrahydrofuran; for 5.5h;Reflux; | To a stirred suspension of LiAlH4 (2.73 g, 71.94 mmol) in anhydrous THF (50 mL) was added 2 (10.00 g, 48.03 mmol) as a solid in portions over 30 min. After addition, the resulting reaction mixture was refluxed for 5 h, cooled to room temperature, and quenched with MeOH (20 mL). The resulting suspension was filtered under vacuum, washed in turn with EtOAc (100 mL) and brine, and dried over anhydrous Na2SO4. The organic extracts were concentrated in vacuo to yield a pale yellow oil (3, 7.80 g, 83%). 1H NMR (400 MHz,CDCl3) d 6.79 (d, J 8.1 Hz, 1H, H-5), 6.74 (d, J 6.1 Hz, 2H, H-2 andH-6), 3.86 (s, J 5.7 Hz, 6H, 2 OCH3), 3.67 (t, J 6.2 Hz, 2H,CH2OH), 2.66 (t, J 7.6 Hz, 2H, Ph-CH2), 1.88 (q, J 7.3 Hz, 2H,CH2CH2OH), 1.74 (s, 1H, CH2CH2OH). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
In cyanoacetic acid; | 4-Hydroxyphenethyl 2-cyano-3-(3,4-dihydroxyphenyl)-2-propenoate (Compound 20) After the reduction of 3,4-dimethoxycinnamic acid to 3-(3,4-dimethoxyphenyl)propanol in the usual manner followed by condensation with cyanoacetic acid according to the procedure in Example 3, the product was demethylated with boron trichloride and condensed with 3,4-dihydroxybenzaldehyde to give the following compound. |
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