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Chemical Structure| 114373-88-5 Chemical Structure| 114373-88-5

Structure of 114373-88-5

Chemical Structure| 114373-88-5

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Product Details of [ 114373-88-5 ]

CAS No. :114373-88-5
Formula : C13H16FNO
M.W : 221.28
SMILES Code : O=C(N1CCCCC1)CC2=CC=C(F)C=C2
MDL No. :MFCD03576297

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Application In Synthesis of [ 114373-88-5 ]

* 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 [ 114373-88-5 ]

[ 114373-88-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-89-4 ]
  • [ 459-04-1 ]
  • [ 114373-88-5 ]
YieldReaction ConditionsOperation in experiment
In tetrahydrofuran; at 0 - 20℃; for 18h; Step B: I-[(4-FluorophenyI)acetyl]piperidine4-FluorophenyIacetic acid (280g, 1.82mol) was suspended in 1.9L toluene followed by the careful addition of 185mL thionyl chloride (303g, 2.545mol). The reaction was heated to 1050C for 16hr (overnight). The reaction was allowed to cool to room temperature and the volatiles were removed in vacuo. The crude acid chloride was dissolved in 1.9L THF, cooled to 00C, and 0.72L piperidine (618g, 7.27mol) was added. The reaction vessel was allowed to warm to ambient temperature for 18hr. The mixture was quenched with a saturated solution of aq. NaHCθ3 and extracted several times withEtOAc. The combined organic extracts were washed with brine, dried over Na2SO^ and filtered on a <n="21"/>fritted funnel. The volatiles were removed in vacuo and the crude residue was purified on silica gel and eluted with a mixture of EtOAc/heptanes (0-75% gradient elution). This furnished the title compound. 1H-NMR (CDCI3): δ 1.32-1.42 (m, 2H), 1.48-1.64 (m, 4H), 3.34-3.42 (m, 2H), 3.54-3.60 (m, 2H), 3.69(s, 2H), 6.90-7.05 (m, 2H), 7.18-7.24 (m, 2H) ppm.
4-Fluorophenylacetic acid (28Og, 1.82mol) was suspended in 1.9L toluene followed by the careful addition of 185mL thionyl chloride (303g, 2.545mol). The reaction was heated to 1050C for 16hr (overnight). The reaction was allowed to cool to room temperature and the volatiles were removed in vacuo. The crude acid chloride was dissolved in 1.9L THF, cooled to 00C, and 0.72L piperidine (618g, 7.27mol) was added. The reaction vessel was allowed to warm to ambient temperature for 18hr. The mixture was quenched with a saturated solution of aq. NaHCO3 and extracted several times withEtOAc. The combined organic extracts were washed with brine, dried over Na2SO4, and filtered on a fritted funnel. The volatiles were removed in vacuo and the crude residue was purified on silica gel and eluted with a mixture of EtO Ac/heptanes (0-75% gradient elution). This furnished the title compound. 1H-NMR (CDCI3): δ 1.32-1.42 (m, 2H), 1.48-1.64 (m, 4H), 3.34-3.42 (m, 2H)5 3.54-3.60 (m, 2H), 3.69(s, 2H), 6.90-7.05 (m, 2H), 7.18-7.24 (m, 2H) ppm.
 

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