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Chemical Structure| 126111-14-6 Chemical Structure| 126111-14-6

Structure of 126111-14-6

Chemical Structure| 126111-14-6

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Product Details of [ 126111-14-6 ]

CAS No. :126111-14-6
Formula : C6H9F2NO2
M.W : 165.14
SMILES Code : O=C(OC)[C@H]1NCC(F)(F)C1
MDL No. :MFCD20232867

Safety of [ 126111-14-6 ]

Application In Synthesis of [ 126111-14-6 ]

* 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 [ 126111-14-6 ]

[ 126111-14-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 203866-17-5 ]
  • [ 126111-14-6 ]
YieldReaction ConditionsOperation in experiment
100% With hydrogenchloride; In ethyl acetate; at 20℃; for 4h; A mixture of compound 15-3 (3 g, 11.3 mmol) and a solution of HCl in EtOAc (15 mL, 4 M) was stirred at rt for 4 hours and concentrated in vacuo to give the title compound 15-4 as a white solid (2.27 g, 100%). The compound was characterized by the following spectroscopic data: MS-ESI: m/z 166.14 [M+H]+; and1H NMR (400 MHz, CDCl3): delta 4.70-4.69 (m, 1H), 3.75-3.87 (m, 2H), 3.71 (s, 3H), 2.91-3.00 (m, 1H), 2.70-2.81 (m, 1H).
With trifluoroacetic acid; In dichloromethane; at 20℃; for 1h; To intermediate 5b (300 mg, 1.13 mmol, 1.00 equiv) in diehloromethane (1 mL) was added trifluoroacetic acid (1 mL) and the resulting solution was stirred for 1 h at room temperature. The mixture was then concentrated under reduced pressure to afford 200 mg (crude) of intermediate 5c as a brown oil.
With trifluoroacetic acid; In dichloromethane; at 20℃; for 4h; (0518) <strong>[203866-17-5](S)-1-tert-butyl 2-methyl 4,4-difluoropyrrolidine-1,2-dicarboxylate</strong> (0.472 g) in CH2Cl2 (1 ml) was treated with trifluoroacetic acid (1.4 ml), stirred at ambient temperature for 4 hours, and concentrated. The product was free-based using a MEGA BE-SCX column with 1:1 CH2Cl2/methanol as eluent for the trifluoroacetic acid. The product was released from the column with 5% (7 M ammonia in methanol) in CH2Cl2 as eluent.
  • 2
  • [ 126111-14-6 ]
  • [ 85482-13-9 ]
  • [ 1445984-74-6 ]
YieldReaction ConditionsOperation in experiment
200 mg With potassium carbonate; In acetonitrile; at 20℃; To intermediate 5c (200 mg, 1 ,21 mmol. 1.00 equiv) in CH3CN (5 mL) was added 2-(bromomeihyl)-l,4-dichlorobenzene (288 mg, 1.20 mmol, 1.00 equiv) and potassium carbonate (502 mg, 3.63 mmol, 3.00 equiv) and the resulting solution was stirred overnight at room temperature. The mixture was diluted with 50 mL of ethyl acetate, washed with 2x30 mL of brine, the organic layer dried over anhydrous sodium sulfate, concentrated, and then purified via silica gel chromatography (petroleum ether/ethyl acetate, 50:1) to afford 200 mg (51%) of intermediate 5d as a yellow oil.
 

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