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Chemical Structure| 52273-55-9

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Product Details of [ 52273-55-9 ]

CAS No. :52273-55-9
Formula : C9H11BrO
M.W : 215.09
SMILES Code : OC1=CC=C(CCCBr)C=C1
MDL No. :MFCD09744419

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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 [ 52273-55-9 ]

[ 52273-55-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 52273-55-9 ]
  • [ 5382-17-2 ]
  • [ 841200-90-6 ]
YieldReaction ConditionsOperation in experiment
90% With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 60℃; for 18.0h; A solution of 4-(3-bromo-propyl)-phenol (EXAMPLE 6; 1.42 g, 6.6 mmol), <strong>[5382-17-2]4-hydroxypiperidine hydrochloride</strong> (908 mg, 6.6 mmol), and N,N-diisopropylethyamine (2.2 mL, 12.3 mmol) in CH3CN (20 mL) was stirred at 60° C. for 18 h. The reaction mixture was cooled to room temperature, and the solvent was removed under reduced pressure to yield an off-white solid. This material was dissolved in CH2Cl2 (200 mL), and the solution was washed with H2O (2.x.50 mL), dried (Na2SO4), filtered and concentrated under reduce pressure to yield a white solid. Diethyl ether was added, and the title compound was collected by filtration (1.4 g, 90percent yield). TLC (SiO2, 5percent 2 M NH3 in CH3OH/CH2Cl2): Rf=0.05. MS (ESI): mass calculated for C14H21NO2, 235.16; m/z found, 236.2 [M+H]+. 1H NMR (400 MHz, CD3OD): 6.96-6.94 (m, 2H), 6.64-6.61 (m, 2H), 3.89-3.82 (m, 1H), 3.29-3.20 (m, 4H), 3.02-2.95 (m, 4H), 2.52 (t, J=7.4, 2H), 1.95-1.87 (m, 4H), 1.68-1.60 (m, 2H).
90% With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 60℃; for 18.0h; EXAMPLE 36; 1- {3- [4- (BENZOOXAZOL-2-YLOXY)-PHENYL]-PROPYL}-PIPERIDIN-4-OL; A. 1-F3- 4-HVDROXV-PHENYL)-PROPY]-PIPERIDIN-4-OL; A SOLUTION of 4- (3-bromo- propyl)-phenol (EXAMPLE 6; 1.42 g, 6.6 MMOL), <strong>[5382-17-2]4-hydroxypiperidine hydrochloride</strong> (908 mg, 6.6 mmol), and N, N-diisopropylethyamine (2.2 mL, 12.3 MMOL) in CH3CN (20 mL) was stirred at 60 °C for 18 h. The reaction mixture was cooled to room temperature, and the solvent was removed under reduced pressure to yield an off-white solid. This material was dissolved in CH2CI2 (200 mL), and the solution was washed with H20 (2 x 50 mL), dried (Na2SO4), filtered and concentrated under reduce pressure to yield a white solid. Diethyl ether was added, and the title compound was collected by filtration (1.4 g, 90percent yield). TLC(SiO2, 5percent 2 M NH3 in CH3OH/CH2Cl2) : Rf = 0. 05. MS (ESI) : mass calculated for C14H21NO2, 235.16 ; m/z found, 236.2 [M+H] +. H NMR (400 MHz, CD30D) : 6.96-6. 94 (m, 2H), 6.64-6. 61 (m, 2H), 3.89-3. 82 (m, 1 H), 3.29- 3.20 (m, 4H), 3.02-2. 95 (m, 4H), 2.52 (t, J = 7.4, 2H), 1.95-1. 87 {M, 4H), 1.68- 1.60 (m, 2H)
 

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