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Chemical Structure| 78104-88-8 Chemical Structure| 78104-88-8

Structure of 78104-88-8

Chemical Structure| 78104-88-8

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Product Details of [ 78104-88-8 ]

CAS No. :78104-88-8
Formula : C5H7N
M.W : 81.12
SMILES Code : CC1(CC1)C#N
MDL No. :MFCD14706015

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Application In Synthesis of [ 78104-88-8 ]

* 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 [ 78104-88-8 ]

[ 78104-88-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15910-91-5 ]
  • [ 78104-88-8 ]
YieldReaction ConditionsOperation in experiment
To a solution of <strong>[15910-91-5]1-methylcyclopropanecarboxylic acid amide</strong> (1.50g, 15.13mmol) in THF (225mL), cooled to 0C, was added pyridine (2.5mL, 30.26mmol) and the reaction was stirred at this temperature for 1 h. TFAA (10.5mL, 75.66mmol) was then added to the mixture, in one portion, and the reaction continued to stir at 0C for 15 min. Sat. NaHC03 solution was added, until pH 8 was reached, and then the mixture was diluted with DCM. The organic phase was separated, and the aqueous phase was extracted with DCM (x 2). Organic fractions were combined, dried (Na2S04) and the solvent removed in vacuo to afford the intermediate product 1-methylcyclopropanecarbonitrile.
With trifluoroacetic anhydride; In tetrahydrofuran; at 60℃; for 12h;Sealed tube; 1-Methylcyclopropane-1-carbonitrile In a 30-mL sealed tube, <strong>[15910-91-5]1-methylcyclopropane-1-carboxamide</strong> (800 mg, 8.07 mmol, 1.00 equiv) was dissolved in tetrahydrofuran (20 mL), to which was added TFAA (8.4 g, 39.99 mmol, 4.96 equiv) at room temperature. The resulting solution was then stirred for 12 h at 60 C. After the reaction was done, the reaction mixture was concentrated under reduced pressure and the residue was dissolved in 5 mL water. The pH value of the resulting mixture was adjusted to 8 using sat. sodium bicarbonate solution and the mixture was extracted with dichloromethane (3*30 mL). The organic layers were combined, dried over sodium sulfate and concentrated under reduced pressure to afford 1-methylcyclopropane-1-carbonitrile (2 g, crude) as yellow oil.
 

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