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Chemical Structure| 128619-83-0 Chemical Structure| 128619-83-0

Structure of 128619-83-0

Chemical Structure| 128619-83-0

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Product Details of [ 128619-83-0 ]

CAS No. :128619-83-0
Formula : C8H11BrS
M.W : 219.14
SMILES Code : CCCCC1=CC=C(Br)S1
MDL No. :MFCD20486050

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Application In Synthesis of [ 128619-83-0 ]

* 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 [ 128619-83-0 ]

[ 128619-83-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1455-20-5 ]
  • [ 128619-83-0 ]
YieldReaction ConditionsOperation in experiment
89% With N-Bromosuccinimide; In N,N-dimethyl-formamide; at 20℃; for 12.1667h; In a 300mL three-neck flask having a dropping funnel, <strong>[1455-20-5]2-butylthiophene</strong> (compound indicated by "2a") (6.0g, 42memol), 2-dodecylthiophene (compound indicated by "2b") (20g, 79mmol), or 2-cetylthiophene (compound indicated by "2c") (13g, 45mmol) was dissolved in DMF (150mL). Then, a solution obtained by dissolving NBS (7.6g, 42mmol; 14.1g, 79mmol; or 8.05g, 45mmol) in DMF (50mL) was added in drops at a room temperature over 10 minutes and stirred at a room temperature for 12 hours. The reaction solution thus obtained was added with a saturated sodium hydrogen carbonate solution (150mL), stirred for 30 minutes, and added with hexane (80mL). Then, a water layer separated was extracted with hexane (80mL×2). After that, organic layers were collected, washed with water (100mL×3), and dried with anhydrous sulfate magnesium. The resulting solution was filtered, and a solvent was removed therefrom under a reduced pressure. As a result, obtained was a compound indicated by "3a" (8.8g, 89% yield) which is in the form of liquid, a compound indicated by "3b" (24.8g, 95% yield) which is in the form of faint yellow liquid, or a compound indicated by "3c" (15.8g, 91% yield) which is in the form of a white solid.(Data of 2-Bromo-5-butylthiophene) 1H-NMR (CDCl3) delta6.60 (1H, t, J=0.8Hz), 2.82 (2H, t, J=8.0Hz), 1.66 (2H, quint, J=8.0Hz), 1.39 (2H, sext, J=8.0Hz), 0.93 (3H, t, J=7.6Hz); EI-MS, m/z=218 (M+)(Data of 2-Brozno-5-dodecyltkxiophene) 1H-NMR (CDCl3) delta6.84 (1H, d, J=3.6Hz), 6.53 (1H, dt, J=3.6Hz, 1.2Hz), 2.73 (2H, t, J=7.6Hz), 1.58-1.64 (2H, m), 1.20-1.35 (18H, m), 0.88 (3H, t, J=7.2Hz); EI-MS, m/z=332 (M+)(Data of 2-Bromo-5-cetylthiophene) Melting point 31-32C; 1H-NMR (CDCl3) delta6.84 (1H, d, J=3.6Hz), 6.52 (1H, d, J=3.6Hz), 2.73 (2H, t, J=8.0Hz), 1.62 (2H, quint, J=8.0Hz), 1.38-1.15 (26H, m), 0.87 (3H, t, J=7.2Hz); EI-MS, m/z=386 (M+)
With bromine; In chloroform; EXAMPLE 32 2-Bromo-5-butylthiophene Bromine, 5 ml (15.63 g or 0.0977 mol), was added to a solution of 15.2 g (0.108 mol) of <strong>[1455-20-5]2-butylthiophene</strong> in 400 ml of chloroform. Following the addition, the mixture was stirred for 10 minutes at room temperature and was then washed with 10% aqueous sodium carbonate solution. The organic layer was separated, dried and evaporated and the remaining oil was distilled under high vacuum to yield a colorless oil. Nmr (CDCl3): 0.89 ppm (t, 3, J=7.5 Hz, CH3). 1.2-1.7 (m, 4, CH2 CH2), 2.7 (t, 2, J=7.5 Hz, CH2). 6.47 (d, 1, J=4 Hz. C4-H), 6.78 (d, 1, J=4 Hz. C3-H).
 

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