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Chemical Structure| 150114-69-5 Chemical Structure| 150114-69-5

Structure of 150114-69-5

Chemical Structure| 150114-69-5

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Product Details of [ 150114-69-5 ]

CAS No. :150114-69-5
Formula : C11H12O5
M.W : 224.21
SMILES Code : O=CC(C1=CC(OC)=C(OC)C(OC)=C1)=O
MDL No. :MFCD05664097

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Application In Synthesis of [ 150114-69-5 ]

* 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.

  • Downstream synthetic route of [ 150114-69-5 ]

[ 150114-69-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 150114-69-5 ]
  • [ 70733-25-4 ]
  • [ 1092500-71-4 ]
YieldReaction ConditionsOperation in experiment
In ethanol; at 60℃; for 1.0h; A round bottom flask is charged with 1g (4.97 mmol) 3-Bromo-5-methyl-benzene-1 ,2- diamine and solved into 27 ml EtOH. 1.23 g (4.97 mmol) 3,4,5-trimethylphenylglyoxal monohydrate is then added and the mixture is heated to 600C for 1 h. After cooling to O0C, <n="111"/>the title compound is collected by filtration and used in the next step without further purification.
  • 2
  • [ 150114-69-5 ]
  • [ 2293-07-4 ]
  • 1-(4-methoxyphenyl)-2-thioxo-5-(3,4,5-trimethoxyphenyl)imidazolidin-4-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
86% With hydrogenchloride; acetic acid; In water; at 50℃; for 1h; General procedure: The target compounds were synthesized employing literatures.41,42 Briefly, to a stirred acetic acid (6 mL) solution of the 2-oxo-2-arylacetaldehyde (2, 1 mmol) and arylurea or arylthiourea(4, 1 mmol), was added conc. HCl (0.2 mL). The mixture was heatedat 50 C for 1 h before it was concentrated. The residue was purifiedby recrystallization from MeOH/DCM or by silica gel columnchromatography.
86% With hydrogenchloride; acetic acid; In water; at 50℃; for 1h; 2-(3,4,5-Trimethoxyphenyl)-2-oxoacetaldehyde (3a, 0.22 g, 1 mmol) and p-methoxyphenylthiourea (4b, 0.18 g, 0.1 mmol) were placed in 50 mL Add acetic acid (6mL) to the eggplant bottle. Concentrated hydrochloric acid (0.2 mL) was added with stirring, and the mixture was stirred at 50 C for 1 hour. After the reaction is completed, the reaction solution is evaporated to dryness under reduced pressure, and purified by silica gel (300-400 mesh) column chromatography. Eluent: petroleum ether - ethyl acetate (1:1), The yellow syrup (5) was obtained in an amount of 0.33 g, and the yield was 86%.
 

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