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Chemical Structure| 639816-37-8 Chemical Structure| 639816-37-8

Structure of 639816-37-8

Chemical Structure| 639816-37-8

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Product Details of [ 639816-37-8 ]

CAS No. :639816-37-8
Formula : C13H10O3S
M.W : 246.28
SMILES Code : O=C(OC)C1=CC=C(C2=CC=C(C=O)S2)C=C1
MDL No. :MFCD06200909

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Application In Synthesis of [ 639816-37-8 ]

* 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 [ 639816-37-8 ]

[ 639816-37-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 639816-37-8 ]
  • [ 174623-07-5 ]
YieldReaction ConditionsOperation in experiment
78% With water; lithium hydroxide; In tetrahydrofuran; at 20℃; for 8h; To a solution of methyl 4-(5-formylthiophen-2-yl)benzoate (25.2, 1.50 g, 6.0 mmol) in THF (15 mL), LiOH (0.439 g, 18.2 mmol) dissolved in water (2.0 mL) was added at room temperature and stirred for 8 h. After completion, THF was removed under reduced pressure, water (30 mL) was added and pH was adjusted to 7 by addition of citric acid solution. The precipitated solid was collected by filtration and the product was purified by washings with diethyl ether and pentane to afford 4-(5-formylthiophen-2-yl)benzoic acid (25.1) as yellow solid.Yield: 1.10 g, 78.0%.
53% With hydrogenchloride; lithium hydroxide; In methanol; water; B. 4-(5-Formyl-thiophene-2-yl)-benzoic Acid To a solution of 4-(5-formyl-thiophene-2-yl)-benzoic acid methyl ester (369 mg, 1.5 mmol) in methanol (50 ml) and water (10 ml) was added lithium hydroxide (205 mg, 5 mmol). After stirring at room temperature for 24 hours, the solution was acidified to pH 2 by addition of 0.1 M hydrochloric acid and extracted with ethyl acetate (4*20 ml). The combined organic extracts were dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel eluding with 10% methanol-dichloromethane to provide 4-(5-formyl-thiophene-2-yl)-benzoic acid (185 mg, 53% yield).
 

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