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CAS No. : | 1889-71-0 | MDL No. : | MFCD00016342 |
Formula : | C14H11ClO | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | DXVALSKCLLBZEB-UHFFFAOYSA-N |
M.W : | 230.69 | Pubchem ID : | 233840 |
Synonyms : |
|
Signal Word: | Danger | Class: | 9 |
Precautionary Statements: | P261-P272-P280-P305+P351+P338-P310-P302+P352-P363-P403-P501 | UN#: | 3077 |
Hazard Statements: | H317-H318 | 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 |
---|---|---|
7.8% | With hydrogenchloride; In ethanol; water;Reflux; | [00181] A mixture of l-(4-chlorophenyl)-2-phenylethanone (350 mg, 1.52mmol), 3- ethoxy-4-hydroxy-5-nitrobenzaldehyde (320 mg, 1.52mmol), and urea (272 mg, 4.53mmol) in anhydrous EtOH (15 mL) was added concentrated HCl solution (0. 5 mL), and the reaction mixture was refluxed for overnight. TLC (EtOAc:MeOH=10: l) showed that about 30% of starting materials were consumed, and the reaction mixture was concentrated. The residue was purified by column chromatography (EtOAc:MeOH=40: l) and preparative HPLC to afford the product Compound 36 as a yellow solid (55.1 mg, yield: 7.8%). 1H NMR (DMSO- 6 400 MHz): delta 10.30 (s, 1H), 8.79 (s, 1H), 7.55 (s, 1H), 7.42 (s, 1H), 7.30 (d, J = 8.4 Hz, 2H), 7.20 (d, J = 8.4 Hz, 2H), 7.18 (s, 1H), 7.00-7.10 (m, 3H), 6.82 (d, J = 7.2 Hz, 2H), 5.20 (d, J = 2.4 Hz, 1H), 4.00-4.10 (m, 2H), 1.33 (t, J = 6.8 Hz, 3H); MS (ESI): m/z 466.0 [M+l]+. |
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