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Chemical Structure| 136321-96-5 Chemical Structure| 136321-96-5

Structure of 136321-96-5

Chemical Structure| 136321-96-5

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Product Details of [ 136321-96-5 ]

CAS No. :136321-96-5
Formula : C17H27BO2
M.W : 274.21
SMILES Code : CCCCCC1CCC(C2=CC=C(B(O)O)C=C2)CC1

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Application In Synthesis of [ 136321-96-5 ]

* 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 [ 136321-96-5 ]

[ 136321-96-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 175278-30-5 ]
  • [ 136321-96-5 ]
  • C25H33Br [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% With tetrakis(triphenylphosphine) palladium(0); tetrabutylammomium bromide; potassium carbonate; In water; isopropyl alcohol; toluene; at 80℃; for 6h; The compound (T-90) (21.1 g), tetrakistriphenylphosphine palladium (0.74 g), potassium carbonate (17.7 g), tetrabutylammonium bromideBromo-2-ethyl-1-iodobenzene (20.0 g),Toluene (200 ml), IPA (150 ml) and H2O (50 ml) were placed in the reactor and stirred at 80 ° C for 6 hours.After the insolubles were removed, the reaction mixture was poured into water and the aqueous layer was extracted with toluene.The organic layer formed simultaneously with water washing was dried over anhydrous magnesium sulfate.The solution was concentrated under reduced pressure and the residue was purified by silica gel chromatography (volume ratio, heptane: toluene = 4: 1) to obtain compound (T-91) (22.6 g; 85percent).
80% With tetrakis(triphenylphosphine) palladium(0); tetrabutylammomium bromide; potassium carbonate; In water; isopropyl alcohol; toluene; at 90℃; for 5h; Compound (T-1) (10.0 g), <strong>[175278-30-5]4-bromo-2-ethyl-1-iodobenzene</strong> (13.6 g), Tetrakis (triphenylphosphine) palladium(2.1 g), potassium carbonate (10.1 g), tetrabutylammonium bromide (1.18 g) and toluene (300 ml), IPA (80 ml) and pure water (20 ml) were charged into a reactor And the mixture was stirred at 90 ° C. for 5 hours. The reaction mixture was poured into water and the aqueous layer was extracted with toluene. The combined organic layers were washed with brine and dried over anhydrous magnesium sulfate. The solution was concentrated under reduced pressure, and the residue was purified by silica gel chromatography (volume ratio, heptane: toluene = 4: 1). (T-2) (12.6 g; 80percent) was obtained by further recrystallization from a mixed solvent of heptane and toluene (volume ratio, 4: 1).
 

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