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Chemical Structure| 1360568-90-6 Chemical Structure| 1360568-90-6

Structure of 1360568-90-6

Chemical Structure| 1360568-90-6

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Product Details of [ 1360568-90-6 ]

CAS No. :1360568-90-6
Formula : C9H14F2O2
M.W : 192.20
SMILES Code : O=C(C1(C)CCC(F)(F)CC1)OC

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Application In Synthesis of [ 1360568-90-6 ]

* 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 [ 1360568-90-6 ]

[ 1360568-90-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 121629-14-9 ]
  • [ 74-88-4 ]
  • [ 1360568-90-6 ]
YieldReaction ConditionsOperation in experiment
Step 2: Synthesis of methyl 4,4-difluoro-l-methylcyclohexanecarboxylate:To a solution of diisopropylamine (11 ml) in tetrahydrafuran (50 ml), n-BuLi (26 ml) was added at 0 C and the reaction mixture was allowed to stir at same temperature for about 10-15 minutes. The reaction mixture was stirred at room temperature for about 45 minutes. Methyl 4,4-difluorocyclohexanecarboxylate (step 1, 5.3 g) in tetrahydrafuran (40 ml) was added drop-wise to above mixture at -78 C. The reaction mixture was stirred at same temperature for about 2 hours and then methyl iodide was added drop-wise. The reaction was maintained at -78 C for an hour and allowed to attain room temperature. Reaction mixture was stirred overnight at room temperature and quenched at 0 C with saturated aq. NH4C1 solution and the compound was extracted with ethyl acetate. The organic layer was washed with saturated brine solution, dried over anhydrous Na2S04 and concentrated then crude product was directly used for the next step. 1H NMR (CDC13, 300 MHz): δ 3.71 (s, 3H), 2.20- 2.16 (m, 2H), 1.96- 1.71 (m, 4H), 1.57- 1.47 (m, 2H), 1.22 (s, 3H).
 

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