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Chemical Structure| 208242-25-5 Chemical Structure| 208242-25-5

Structure of 208242-25-5

Chemical Structure| 208242-25-5

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Product Details of [ 208242-25-5 ]

CAS No. :208242-25-5
Formula : C6H7F3O2
M.W : 168.11
SMILES Code : O=C(C1(C(F)(F)F)CC1)OC
MDL No. :MFCD06801321
InChI Key :PAWUSHZXEZPDBE-UHFFFAOYSA-N
Pubchem ID :24208784

Safety of [ 208242-25-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H301-H315-H319-H335
Precautionary Statements:P261-P301+P310-P305+P351+P338
Class:3(6.1)
UN#:1992
Packing Group:

Application In Synthesis of [ 208242-25-5 ]

* 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 [ 208242-25-5 ]

[ 208242-25-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 208242-25-5 ]
  • [ 371917-17-8 ]
YieldReaction ConditionsOperation in experiment
64% With diisobutylaluminium hydride; In dichloromethane; at 0℃; for 2h; [1691] At oo C., 26.7 ml (26.7 mmol) of diisobutylaluminumhydride (1M in dichloromethane) were slowly addeddropwise to a solution of 1.89 g (10.7 mmol) of methyl1-(trifluoromethyl)cyclopropanecarboxylate in 10 ml ofdichloromethane. The mixture was then stirred at oo C. foranother 2 hand the reaction was subsequently terminated byaddition of 10 ml of methanol. The reaction mixture wasdiluted with 30 ml of aqueous 20% strength sodium potassiumtartrate solution and 30 ml of aqueous buffer solution(pH 7) and stirred vigorously at room temperature overnight.The phases were separated and the aqueous phase wasextracted three times with dichloromethane. The combinedorganic phases were dried over magnesium sulphate and filtered,and the solvent was removed under reduced pressure.The crude product corresponded to the title compound. Yield:0.96 g (64% of theory)[1692] 1H-NMR (400 MHz, CDCI3 ): ll [ppm]=3.74 (d,2H), 1.65 (t, lH), 1.06-1.02 (m, 2H), 0.81-0.76 (m, 2H).
EXAMPLE 11; 1-(Methylsulfonyl)-4-(4-(1-(1-((1-(trifluoromethyl)cyclopropyl)methyl)piperidin-4-yl)ethoxy)phenyl)-1,2,3,6-tetrahydropyridine 1. (1-(Trifluoromethyl)cyclopropyl)methanolTo an ice-cold suspension of lithium aluminum hydride (33.91 mmoles; 1.29 g) in diethyl ether (90 mL) is added dropwise over 25 minutes methyl 1-(trifluoromethyl)cyclopropanecarboxylate (16.95 mmoles; 3.00 g) in 30 mL of diethylether. The reaction is stirred at 0 C. for 2 hours. The mixture is quenched by slow addition of 7.5 mL of water, then 15 mL of 5 M sodium hydroxide and 9 mL of water. The thick slurry is vigourously stirred at room temperature for 3 hours. The mixture is transferred to a separatory funnel, diluted with water and extracted with diethylether. The combined organic layers are washed with brine, dried over magnesium sulfate, filtered and concentrated to dryness. 2.37 g of the title compound as a colorless oil are obtained. 2.37 g. 1H NMR (CDCl3) d (ppm): 0.762-0.807 (m, 2H), 1.018-1.055 (m, 2H), 3.732 (s, 2H).
0.96 g With diisobutylaluminium hydride; In methanol; dichloromethane; at 0℃; for 2h; At 0 C, 26.7 ml (26.7 mmol)of diisobutylaluminium hydride (1M in dichloromethane) were slowly addeddropwise to a solution of 1.89 g (10.7 mmol) of methyl1-(trifluoromethyl)cyclopropanecarboxylate in 10 ml of dichloromethane. Themixture was then stirred at 0 C for another 2 h and the reaction wassubsequently terminated by addition of 10 ml of methanol. The reaction mixturewas diluted with 30 ml of aqueous 20% strength sodium potassium tartratesolution and 30 ml of aqueous buffer solution (pH 7) and stirred vigorously atroom temperature overnight. The phases were separated and the aqueous phase wasextracted three times with dichloromethane. The combined organic phases weredried over magnesium sulphate and filtered, and the solvent was removed underreduced pressure. The crude product corresponded to the title compound. Yield:0.96 g (64% of theory)
 

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