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Chemical Structure| 41876-68-0 Chemical Structure| 41876-68-0

Structure of 41876-68-0

Chemical Structure| 41876-68-0

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Product Details of [ 41876-68-0 ]

CAS No. :41876-68-0
Formula : C16H23N
M.W : 229.36
SMILES Code : C#CC1=CC=C(N(CCCC)CCCC)C=C1
English Name :N,N-Dibutyl-4-ethynylaniline

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Application In Synthesis of [ 41876-68-0 ]

* 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 [ 41876-68-0 ]

[ 41876-68-0 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 636-31-7 ]
  • [ 41876-68-0 ]
  • [ 667865-46-5 ]
YieldReaction ConditionsOperation in experiment
79% With copper(l) iodide; diisopropylamine In tetrahydrofuran at 20℃; for 12h;
460 mg With copper(l) iodide; tetrakis(triphenylphosphine) palladium(0); diisopropylamine In tetrahydrofuran at 40℃; for 12h;
  • 2
  • [ 51554-95-1 ]
  • [ 41876-68-0 ]
  • [ 1830439-88-7 ]
YieldReaction ConditionsOperation in experiment
60% With bis-triphenylphosphine-palladium(II) chloride; copper(l) iodide; triethylamine In tetrahydrofuran at 80℃; for 10h; Inert atmosphere; 2.2.5. Synthesis of N,N-dibutyl-4-((4-pentylphenyl)ethynyl)aniline (b3) a4 (0.137 g, 0.600 mmol) and 1-bromo-4-pentylbenzene(0.113 g, 0.500 mmol) were dissolved in TEA (150 mL) and THF(150 mL). The solutionwas flushed with bubbling Ar gas for 30 min.Then the Pd(PPh3)2Cl2 (12.6 mg, 0.0180 mmol) and CuI (5.7 mg,0.030 mmol) were added. The reaction mixture was then stirred at80 C for 10 h under Ar atmosphere. The resulting mixture wasconcentrated, diluted with CH2Cl2, and filtered through a plug ofsilica gel. The solvent was removed under vacuum and the productwas purified by column chromatography (SiO2, petroleum ether/CH2Cl2 7:1) to give b3 (0.135 mg, 60%) as a yellow oil liquid. 1HNMR (CDCl3, 500 MHz): d 0.94 (t, J 6.0 Hz, 3H),1.00 (t, J 7.0 Hz,6H), 1.39 (m, 8H), 1.68 (m, 6H), 2.65 (t, J 7.5 Hz, 2H), 3.33 (t,J 7.5 Hz, 4H), 6.62 (d, J 9.0 Hz, 2H), 7.17 (d, J 7.5 Hz, 2H), 7.40(d, J 9.0 Hz, 2H), 7.45 (d, J 7.5 Hz, 2H) ppm. FT-IR (KBr): y 2935,2850, 2200, 1601, 1503, 1367, 1184, 112, 792, 731, 535 cm1. MALDITOF-MS (dithranol): m/z: calc'd for C27H37N: 375.29 g/mol, found:376.2 g/mol [MH]. Elemental analysis calc'd (%) for C27H37N(375.29): C 86.34, H 9.93, N 3.73; found: C 86.35, H 9.94, N 3.74.
60% With tetrakis(triphenylphosphine) palladium(0); triethylamine; copper(l) chloride In tetrahydrofuran at 80℃; for 10h; Inert atmosphere; 3.6 2.3.5 N,N-Dibutyl-4-((4-pentylphenyl)ethynyl)aniline (b2) b2 (37.5 mg, 0.1 mmol) and click reagent TCNE (12.8 mg, 0.1 mmol) were dissolved in THF (2 mL). After the reaction mixture was then stirred at 40 °C for 2 h under Ar. The solvent was removed in vacuo, and the product was purified by column chromatography (SiO2, CH2Cl2) to give c4 (44.8 mg, 89%) as a black-red solid. 1H NMR (CDCl3, 500 MHz): δ=0.92 (m, 3H), 1.04 (m, 6H), 1.36 (m, 4H), 1.43 (m, 4H), 1.63 (m, 2H), 1.67 (m, 4H), 2.70 (m, 2H), 3.40 (m, 4H), 6.69 (d, J=9.0 Hz, 2H), 7.35 (d, J=8.0 Hz, 2H), 7.70 (d, J=8.0 Hz, 2H), 7.80 (d, J=9.0 Hz, 2H) ppm FTIR (KBr): υ=2935, 2850, 2187, 1613, 1477, 1343, 1184, 816 cm-1. MALDI-TOF-MS (dithranol): m/z: calcd for C33H37N5: 503.30 g/mol, found: 504.2 g/mol [MH]+. Elemental analysis calcd (%) for C33H37N5: C 78.69, H 7.40, N 13.90; found: C 78.68, H 7.43, N 13.89.
  • 3
  • [ 41876-68-0 ]
  • [ 4714-24-3 ]
  • [ CAS Unavailable ]
YieldReaction ConditionsOperation in experiment
55 % With copper(l) iodide; N-ethyl-N,N-diisopropylamine at 60℃; Inert atmosphere; 4.2.1. Preparation of compound M N,N-dibutyl-4-ethynylaniline obtained from previous work [33] (1.648 g, 0.0072 mmol), 1-bromo-4-styrylbenzene (0.774 g, 0.003 mol), [PdCh (PPh3)] (0.120 mg, 0.00017 mmol), CuI (0.034 g, 0.00017 mol) are put into a bottle, then add iPrNH as solvent, shaking for 36 h at 60 °C. After the temperature drops to room temperature, the solvent is cleared, then the separation technology column chromatography, the eluent is CH2Cl2, and the first crude purification is performed to remove the catalyst in the system. And then use a chromatographic column (SiO2, VDCM) for purification to give M(803.5 mg, 55%), as a light-yellow solid. 1H NMR (400 MHz, CDCl3, d): 7.58-7.53 (m, 4H), 7.50 (s, 8H), 7.39 (m, 8H), 7.33-7.25 (m, 4H), 7.13 (d, J 2.8 Hz, 4H), 6.65-6.60 (m, 4H), 3.40-3.18 (m, 8H),1.66-1.56 (m, 8H),1.40 (m, 8H), 0.99 (m, 12H). IR (neat): 2955, 2937, 2860, 2206,1608,1526,1363,1191,1109, 964, 827, 751, 681, 537. MALDI-TOF-MS (dithranol): m/z: [MH]+ calcd for C30H33N: 407.26, found: 408.96. Elemental analysis calcd (%) for C30H33N (407.26): C 88.40, N 3.44, H 8.16, found: C 88.38, N 3.44, H 8.18.
 

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