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Chemical Structure| 179898-22-7 Chemical Structure| 179898-22-7

Structure of 179898-22-7

Chemical Structure| 179898-22-7

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Product Details of [ 179898-22-7 ]

CAS No. :179898-22-7
Formula : C12H15NO
M.W : 189.25
SMILES Code : OC1=CC2=C(C=C1)C(C)=CC(C)(C)N2
MDL No. :MFCD15525601

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Application In Synthesis of [ 179898-22-7 ]

* 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 [ 179898-22-7 ]

[ 179898-22-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 179898-22-7 ]
  • [ 18791-75-8 ]
  • hyroxylamine-O-sulfonic acid [ No CAS ]
  • [ 18791-99-6 ]
YieldReaction ConditionsOperation in experiment
0.50 g (51%) With sodium hydroxide; In water; acetonitrile; 4-Bromo-2-cyanothiophene To a solution of 4-bromo-2-thiophenecarboxaldehyde (1.0 g, 5.2 mmol, Aldrich) in acetonitrile/water (20 mL/2 mL) was added hyroxylamine-O-sulfonic acid (2.4 g, 21.2 mmol, Aldrich). The dark solution was heated to 65 C. with stirring. After 8 h, the reaction was quenched with 10% NaOH (10 mL). The solution was extracted with EtOAc (30 mL). The organic layer was washed with water and brine (3*10 mL each), dried (Na2 SO4), and concentrated in vacuo to afford the crude product as a tan solid. The crude product was purified by silica flash chromatography (5-25% EtOAc:hexane) to afford 0.50 g (51%) of 4-bromo-2-cyanothiophene as a white solid.
0.50 g (51%) With sodium hydroxide; In water; acetonitrile; 4-Bromo-2-cyanothiophene. To a solution of 4-bromo-2-thiophenecarboxaldehyde (1.0 g, 5.2 mmol, Aldrich) in acetonitrile/water (20 mL/2 mL) was added hyroxylamine-O-sulfonic acid (2.4 g, 21.2 mmol, Aldrich). The dark solution was heated to 65 C. with stirring. After 8 h, the reaction was quenched with 10% NaOH (10 mL). The solution was extracted with EtOAc (30 mL). The organic layer was washed with water and brine (3*10 mL each), dried (Na2 SO4), and concentrated in vacuo to afford the crude product as a tan solid. The crude product was purified by silica flash chromatography (5-25% EtOAc:hexane) to afford 0.50 g (51%) of 4-bromo-2-cyanothiophene as a white solid.
 

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