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Chemical Structure| 851634-59-8 Chemical Structure| 851634-59-8

Structure of 851634-59-8

Chemical Structure| 851634-59-8

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Product Details of [ 851634-59-8 ]

CAS No. :851634-59-8
Formula : C9H12OS
M.W : 168.25
SMILES Code : OCC1=CSC2=C1CCCC2
MDL No. :MFCD11597579

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Application In Synthesis of [ 851634-59-8 ]

* 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 [ 851634-59-8 ]

[ 851634-59-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 19156-54-8 ]
  • [ 851634-59-8 ]
YieldReaction ConditionsOperation in experiment
100% With borane-THF; In tetrahydrofuran; at 0 - 20℃; for 2h; <strong>[19156-54-8]4,5,6,7-tetrahydrobenzo[b]thiophene-3-carboxylic acid</strong> (1.0 g, 5.5 mmol) was dissolved in THF (11 mL) and borane·THF (0.94 mg, 0.95 M in THF solution , 11 mmol) at 0 C., and the mixture was stirred at room temperature for 2 hours. Water was added to the reaction solution at 0 C., and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous sodium sulfate and concentrated to give a crude product. The resulting crude product was purified by silica gel column chromatography (n-hexane ? n-hexane / ethyl acetate = 3/1) to give the title compound (0.97 g, colorless transparent oil, quantitative) was obtained
86% With lithium aluminium tetrahydride; In tetrahydrofuran; diethyl ether; at 20℃; for 1.58333h; A solution of <strong>[19156-54-8]4,5,6,7-tetrahydro-1-benzothiophene-3-carboxylic acid</strong> (400 mg, 2.2 mmol) in diethyl ether (10 mL) was added under nitrogen to lithium aluminium hydride (1M solution in tetrahydrofuran, 3 mL, 3 mmol) in diethyl ether (10 mL) dropwise over 5 minutes. The reaction was stirred at room temperature for 1.5 hours then quenched with saturated ammonium chloride solution. The products were extracted into diethyl ether (x3). The combined organic layers were washed with water and brine, dried over MgSO4 and evaporated in vacuo to give 4,5,6,7-tetrahydro-1-benzothien-3-ylmethanol (320 mg, 86%). 1H NMR (500 MHz, CDCl3) delta 6.99 (1H, s), 4.56 (2H, s), 2.76 (2H, t, J=5.5 Hz), 2.58 (2H, t, J=5.6 Hz), 1.86-1.79 (4H, m), 1.43 (1H, s).
 

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