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Chemical Structure| 39868-71-8 Chemical Structure| 39868-71-8

Structure of 39868-71-8

Chemical Structure| 39868-71-8

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Product Details of [ 39868-71-8 ]

CAS No. :39868-71-8
Formula : C10H11Br
M.W : 211.10
SMILES Code : BrC1=CC=C(C2CCC2)C=C1
MDL No. :MFCD19439999

Safety of [ 39868-71-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 39868-71-8 ]

* 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 [ 39868-71-8 ]

[ 39868-71-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 19936-14-2 ]
  • [ 39868-71-8 ]
YieldReaction ConditionsOperation in experiment
100% With triethylsilane; boron trifluoride diethyl etherate; In dichloromethane; at -70 - -10℃; Step 2: (0138) (0139) 13 g (0.057 mol) (1-a) was dissolved in 130 ml dichloromethane, and cooled to -70 C. with stirring. 15 g (0.132 mol) triethyl silicane was added dropwise. Then, 19 g (0.132 mol) boron trifluoride etherate was added dropwise to eliminate the hydroxyl group, whereby the solid was gradually dissolved. After addition, the solution was naturally warmed to -10 C. and poured into 100 ml aqueous sodium carbonate. The organic phase is separated, extracted, washed with water, and purified by silica gel column chromatography, to obtain 12 g of a colorless liquid (1-b) in a quantitative yield.
66% To a solution of 1.37 g of <strong>[19936-14-2]1-(4-bromophenyl)-cyclobutanol</strong> (6 mmol) in 15 ml DCM were added 1.15 ml of triethylsilane (7.2 mmol) and the mixture was cooled to -78 C. Then 1.15 ml of boron trifluoride diethyl etherate complex were added and the reaction mixture was warmed to -40 C. and stirred for 8 h. The reaction was then quenched by addition of 10% aqueous KHCO3 and the mixture was extracted three times with DCM. The combined extracts were washed with brine, dried with magnesium sulfate and concentrated. The remaining residue was purified by column chromatography (silica gel; cyclohexane) to give 0.84 g (66%) of 1-bromo-4-cyclobutyl-benzene as a colorless liquid. 1H NMR (CDCl3, 300 MHz): delta 1.85 (m, 1H), 1.92-2.18 (m, 3H), 2.33 (m, 2H), 3.49 (quint, J=8.5 Hz, 1H), 7.08 (d, J=8.5 Hz, 2H), 7.40 (d, J=8.5 Hz, 2H).
  • 2
  • [ 39868-71-8 ]
  • [ 19936-14-2 ]
 

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