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Chemical Structure| 13141-40-7 Chemical Structure| 13141-40-7

Structure of 13141-40-7

Chemical Structure| 13141-40-7

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Product Details of [ 13141-40-7 ]

CAS No. :13141-40-7
Formula : C15H12O
M.W : 208.26
SMILES Code : OCC1=CC=CC=C1C#CC2=CC=CC=C2
MDL No. :MFCD01924920

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Application In Synthesis of [ 13141-40-7 ]

* 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 [ 13141-40-7 ]

[ 13141-40-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 59046-72-9 ]
  • [ 13141-40-7 ]
YieldReaction ConditionsOperation in experiment
100% With sodium tetrahydroborate; In methanol; at 0℃; for 0.5h; General procedure: NaBH4 (50 mg, 1.3 mmol) was added to a solution of commercial 2-phenoxybenzaldehyde (260 mg, 1.31 mmol) in MeOH (5 mL) at 0 C. After stirring for 30 min at 0 C, the reaction mixture was diluted with water, extracted with EtOAc, dried over MgSO4 and evaporated. The resulting residue was purified by column chromatography on silica gel (n-hexane/EtOAc = 5/1) to provide the title compound (228 mg, 1.14 mmol) in 87% yield as a colorless solid.
95% With sodium tetrahydroborate; In methanol; at 0℃; for 0.333333h; Under nitrogen conditions, 2-bromobenzaldehyde(10 mmol), phenylacetylene (12 mmol), Pd(PPh3)2Cl2(0.2 mmol) and CuI (0.1 mmol) were successively introducedinto a 100-mL two-neck flask equipped with Et3N(40 mL). The resulting mixture was stirred at 50 C for 12 hand monitored with TLC. After completion, the crude mixturewas filtered through celite and Et3Nwas removed undervacuum. The residue was diluted with EtOAc (60 mL) andwashed with water (2 × 50 mL). The organic layer was driedover Na2SO4,which was further purified via column chromatographyon silica gel (the mixture of petroleum ether andEtOAc was used as elute) to give <strong>[59046-72-9]2-(phenylethynyl)benzaldehyde</strong>(1.83 g) in 89% yield. <strong>[59046-72-9]2-(phenylethynyl)benzaldehyde</strong> was dissolved in methanol(30 mL), and the resulting mixture was cooled to 0 C. NaBH4 (5 mmol) was added in portions, and the solutionwas stirred for additional 20 min. The reaction was quenchedwith saturated ammonium chloride solution (30 mL).Methanol was removed under vacuum, and the residue wasextracted by EtOAc (2 × 30 mL). The combined organic layerwas dried over anhydrous Na2SO4.After the solvent wasremoved under reduced pressure, (2-(phenylethynyl)phenyl)methanol 1a was obtained (1.76 g) in 95% yield, which wasused directly for the next cyclization without purification.
88% With sodium tetrahydroborate; In methanol; at 0 - 20℃; General procedure: To a solution of o-alkynyl quinoline aldehydes 2 (1 mmol) or o-alkynyl benzaldehyde 4 in methanol (5 mL) at 0 C was added NaBH4 (2 equiv) slowly over a period of time. After whole of NaBH4 had been added, the reaction mixture was stirred at room temperature. After completion of reaction (monitored by TLC), chilled water was added and solid precipitate was obtained. The solid precipitate was filtered and used as such.
 

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