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Chemical Structure| 1239596-54-3 Chemical Structure| 1239596-54-3

Structure of 1239596-54-3

Chemical Structure| 1239596-54-3

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Product Details of [ 1239596-54-3 ]

CAS No. :1239596-54-3
Formula : C5H9F2NO
M.W : 137.13
SMILES Code : OC1C(F)(F)CNCC1
MDL No. :MFCD16250749

Safety of [ 1239596-54-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1239596-54-3 ]

* 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 [ 1239596-54-3 ]

[ 1239596-54-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 24424-99-5 ]
  • [ 1239596-54-3 ]
  • [ 1209780-71-1 ]
YieldReaction ConditionsOperation in experiment
82.1% In dichloromethane; at 20℃; for 12h;Inert atmosphere; To a solution of B7 (250 mg, 1.8 mmol) in dichloromethane (20 mL) was added di-tert-butyl dicarbonate (392 mg, 1.8 mmol). The reaction mixture was stirred at room temperature under nitrogen for 12 hours. Water was added to the solution and the mixture was extracted with dichloromethane (20 mL). The organic phase was dried over sodium sulfate, filtered, concentrated in vacuo and washed with n-hexane to give the product B8 as a white solid (350 mg, yield 82.1%). 1H NMR (400 MHz, DMSO-d6) 5ppm: 5.76 (d, J = 5.4 Hz, 1H), 4.02 - 3.66 (m, 2H), 3.68 - 3.44 (m, 2H), 3.29 (s, 1H), 1.75 (ddd, J = 11.3, 7.6, 3.8 Hz, 1H), 1.70 - 1.50 (m, 1H), 1.40 (s, 8H)
In dichloromethane; at 20℃; for 2h;Inert atmosphere; ferf-Butyl 3,3-difluoro-4-hydroxypiperidine-1 -carboxylate:In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to a solution of 3,3-difluoropiperidin-4-ol (700 mg, 5.10 mmol) in dry CH2CI2 (50 ml.) was added Boc20 (1 .1 1 g, 5.10 mmol). The reaction mixture was stirred at rt for 2 h. Water was then added, the layers separated and the aq. layer extracted with CH2CI2 (3x). The combined org. extracts were washed with brine, dried over MgS04, filtered, and concentrated under reduced pressure to give the title compound as a yellow solid. LC-MS-conditions 08: tR = 0.69 min; [M-CH3+H]+ = 223.30.
In dichloromethane; at 20℃; for 2h;Inert atmosphere; tert-Butyl 3,3-difluoro-4-hydroxypiperidine-1-carboxylate In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to a solution of 3,3-difluoropiperidin-4-ol (700 mg, 5.10 mmol) in dry CH2Cl2 (50 mL) was added Boc2O (1.11 g, 5.10 mmol). The reaction mixture was stirred at rt for 2 h. Water was then added, the layers separated and the aq. layer extracted with CH2Cl2 (3*). The combined org. extracts were washed with brine, dried over MgSO4, filtered, and concentrated under reduced pressure to give the title compound as a yellow solid. LC-MS-conditions 08: tR=0.69 min; [M-CH3+H]+=223.30.
In dichloromethane; at 20℃; for 2h;Inert atmosphere; In a flame dried round-bottomed flask equipped with a magnetic stir bar and under inert atmosphere (N2), to a solution of 3,3-difluoropiperidin-4-ol (700 mg, 5.10 mmol) in dry CH2CI2 (50 ml_) was added Boc20 (1.1 1 g, 5.10 mmol). The reaction mixture was stirred at rt for 2 h. Water was then added, the layers separated and the aq. layer extracted with CH2CI2 (3x). The combined org. extracts were washed with brine, dried over MgS04, filtered, and concentrated under reduced pressure to give the title compound as a yellow solid. LC-MS-conditions 08: tR = 0.69 min; [M-CH3+H]+ = 223.30.
With triethylamine; In tetrahydrofuran; at 20℃; for 16h; To a suspension of 3,3-difluoropiperidin-4-ol (1g; 5.76mmol) in THF (5ml_) was added triethylamine (0.86 mL; 6.34 mmol) followed by Boc anhydride (1.32g; 6.05mmol), and the mixture was stirred at RT for 16h. The reaction mixture was then diluted with water (100 mL) and extraxted with EtOAc (3x 50 mL), the organic layer was washed with 1N HCI (2 x 30 mL), brine, dried over anhydrous Na2S04, and concentrated to provide the desired product as a white solid . 1H NMR (400 MHz, DMSO-cfe) delta 5.73 (d, J= 5.4 Hz, 1H), 3.91 - 3.63 (m, 2H), 3.61 -3.41 (m, 2H), 3.29 (d, J=4.8Hz, 1H), 1.75 (ddt, J= 15.3, 7.7, 3.8 Hz, 1H), 1.56 (dtt, J= 11.0, 7.0, 3.1 Hz, 1 H), 1 .40 (s, 9H). M/Z (M+H) = 182.1 .

  • 2
  • [ 1067915-34-7 ]
  • [ 1239596-54-3 ]
 

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