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Chemical Structure| 1158651-05-8 Chemical Structure| 1158651-05-8

Structure of 1158651-05-8

Chemical Structure| 1158651-05-8

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Product Details of [ 1158651-05-8 ]

CAS No. :1158651-05-8
Formula : C25H34BNO4
M.W : 423.35
SMILES Code : O=C(OC(C)(C)C)NC1=CC=C(C2=CC=C(B3OC(C)(C)C(C)(C)O3)C=C2CC)C=C1

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* 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 [ 1158651-05-8 ]

[ 1158651-05-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1158651-05-8 ]
  • [ 117635-21-9 ]
  • [ 1158651-06-9 ]
YieldReaction ConditionsOperation in experiment
56% With Aliquat 336; sodium carbonate;tetrakis(triphenylphosphine) palladium(0); In water; toluene; at 90℃; for 48h; 1,4-dibromo-2,5-dihexyl benzene (8.05 mmoles, 3.255g), boronic ester 26 (17.7 mmoles, 7.545g), Na2CO3 (40.3 mmoles, 4.268g) and Aliquat 336 (0.500g) were suspended in toluene (100 mL) in a 250 mL two-necked- round-bottom-flask with stir bar and condenser. The reaction mixture degassed and Pd(PPh3)4 (0.403 mmoles, 0.465g) added followed by addition of degassed water (50 mL). Reaction heated to 90C for two days. Resulting reaction mixture diluted with ethyl acetate (150 mL), washed with ethyl acetate (3 x 100 mL). Organic layer washed with brine (2 x 100 mL), dried over magnesium sulfate, filtered and concentrated. Purification by column chromatography on silica gel using 1 :3 DCM: Hexanes to yield white powder (56%, 3.8g). 1 H NMR (500 MHz, CD2CI2) delta = 7.45 (d, J = 8.5Hz, 4H), 7.33-7.31 (m, 5H), 7.26-7.19 (m, 5H), 6.65 (s, 2H), 2.71 -2.63 (m, 9H0, 1 .54 (s, 18H), 1 .31 -1 .20 (m, 14H), 1 .15 (t, J = 7.49, 7H), 0.83 (t, J = 6.85Hz, 6H).
56% With sodium carbonate;tetrakis(triphenylphosphine) palladium(0); Aliquat 336; In water; toluene; at 90℃; for 48h;Inert atmosphere; 1,4-dibromo-2,5-dihexyl benzene (8.05 mmoles, 3.255 g), boronic ester 7 (17.7 mmoles, 7.545 g), Na2CO3 (40.3 mmoles, 4.268 g) and Aliquat 336 (0.500 g) were suspended in toluene (100 mL) in a 250 mL two-necked-round-bottom-flask with stir bar and condenser. Reaction mixture degassed for 30 minutes. Pd(PPh3)4 (0.403 mmoles, 0.465 g) added as a powder to reaction mixture. Reaction mixture degassed for a further 15 minutes, whilst simultaneously degassing water (50 mL). Water added via syringe to reaction vessel. Reaction heated to 90 C. for two days. Resulting reaction mixture diluted with ethyl acetate (150 mL), washed with ethyl acetate (3×100 mL). Organic layer washed with brine (2×100 mL), dried over magnesium sulfate, filtered and concentrated. Purification by column chromatography on silica gel using 1:3 dichloromethane: Hexanes to yield white powder (56%, 3.8 g). 1H NMR (500 MHz, CD2Cl2) delta=7.45 (d, J=8.5 Hz, 4H), 7.33-7.31 (m, 5H), 7.26-7.19 (m, 5H), 6.65 (s, 2H), 2.71-2.63 (m, 9H), 1.54 (s, 18H), 1.31-1.20 (m, 14H), 1.15 (t, J=7.49, 7H), 0.83 (t, J=6.85 Hz, 6H).
 

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