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Chemical Structure| 865233-41-6 Chemical Structure| 865233-41-6

Structure of 865233-41-6

Chemical Structure| 865233-41-6

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Product Details of [ 865233-41-6 ]

CAS No. :865233-41-6
Formula : C14H16O3
M.W : 232.28
SMILES Code : CC#CC(C1=CC=C(O)C=C1)CC(OCC)=O

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Application In Synthesis of [ 865233-41-6 ]

* 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 [ 865233-41-6 ]

[ 865233-41-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 865233-41-6 ]
  • [ 71831-21-5 ]
  • ethyl 3-(4-(4-(hydroxymethyl)benzyloxy)phenyl)hex-4-ynoate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With caesium carbonate; In N,N-dimethyl-formamide; at 20℃; for 12h;Inert atmosphere; 4.0 g of ethyl 3-(4-hydroxyphenyl)hex-4-inoate prepared in Manufacturing Example 1 and 5.0 g of <strong>[71831-21-5](4-(bromomethyl)phenyl)methanol</strong> prepared in step 1) were loaded in a 500 mL flask containing 50 ml of DMF in nitrogen atmosphere, followed by stirring for dissolving them. Then, 9.0 g of Cs2CO3 was loaded thereto, followed by stirring at room temperature for 12 hours. Upon completion of the reaction, distilled water was slowly added thereto, followed by extraction using ethylacetate. The extract was washed with brine, dried over anhydrous MgSO4, and concentrated. Then, silica gel column chromatography was performed to give the target compound. (0252) 1H NMR (400 MHz, CDCl3): delta 7.42 (2H, d), 7.38 (2H, d), 7.29 (2H, d), 6.93 (2H, d), 5.06 (2H, s), 4.73 (2H, d), 4.15 (2H, m), 4.06 (1H, m), 2.68 (2H, m), 1.84 (3H, s), 1.69 (1H, m), 1.24 (3H, m).
With caesium carbonate; In N,N-dimethyl-formamide; at 20℃; for 12h;Inert atmosphere; Under a nitrogen atmosphere, ethyl 3-(4-hydroxyphenyl)hex-4-ynoate (4.0 g) obtained in Preparative Example 1 and <strong>[71831-21-5](4-(bromomethyl)phenyl)methanol</strong> (5.0 g) obtained in step 1 were added to DMF (50 mL) in a 500-mL flask and stirred to dissolve, followed by adding dropwise Cs2CO3 (9.0 g), and then the mixture was stirred at room temperature for 12 hours. Upon completion of the reaction, distilled water was slowly added dropwise, extracted with ethyl acetate, washed with brine, dried over anhydrous magnesium sulfate, and then concentrated. Thereafter, the reaction product was separated by silica column chromatography to give the title compound. 1H NMR (400MHz, CDCl3): delta 7. 42 (2H, d), 7. 38 (2H, d), 7.29(2H, d), 6.93(2H, d), 5.06(2H, s), 4.73(2H, d), 4.15(2H, m), 4.06(1H, m), 2.68(2H, m), 1.84(3H, s), 1.69(1H, m), 1.24(3H, m).
 

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