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Chemical Structure| 121212-25-7 Chemical Structure| 121212-25-7

Structure of 121212-25-7

Chemical Structure| 121212-25-7

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Product Details of [ 121212-25-7 ]

CAS No. :121212-25-7
Formula : C9H9NO
M.W : 147.17
SMILES Code : NCC1=C2C=COC2=CC=C1
MDL No. :MFCD15145975

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Application In Synthesis of [ 121212-25-7 ]

* 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 [ 121212-25-7 ]

[ 121212-25-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 95333-17-8 ]
  • [ 121212-25-7 ]
YieldReaction ConditionsOperation in experiment
16.2% With sodium tetrahydroborate; nickel dichloride; In methanol; at 20℃; for 2h; Add <strong>[95333-17-8]benzofuran-4-carbonitrile</strong> C1-1e (300 mg, 2.09 mmol) in methanol (50 mL). Nickel chloride (543 mg, 4.19 mmol) was slowly added with sodium borohydride (159 mg, 4.19 mmol) and allowed to react at room temperature for 2 hours. The mixture was filtered through celite, washed with methanol and evaporated. The crude product was purified on silica gel (dichloromethane: methanol = 10: 1), to give benzofuran-4-ylmethylamine C2-1 (50mg, 16.2% yield) as a yellow solid.
16.2% With sodium tetrahydroborate; nickel dichloride; In methanol; at 20℃; for 2h; In a single-necked flask, add <strong>[95333-17-8]benzofuran-4-carbonitrile</strong> C1-1e (300 mg, 2.09 mmol), methanol (50 mL), nickel chloride (543 mg, 4.19 mmol), and slowly add sodium borohydride (159 mg, 4.19 mmol). , 2 hours reaction at room temperature.The mixture was filtered through celite, washed with methanol,The filtrate was concentrated under reduced pressure to obtain a crude product. The crude was purified on silica gel (dichloromethane:Methanol = 10: 1) to give benzofuran-4-ylmethylamine C2-1 (50 mg, 16.2% yield) as a yellow solid.
16.2% With sodium tetrahydroborate; nickel dichloride; In methanol; at 10 - 30℃; for 2h; Add <strong>[95333-17-8]benzofuran-4-carbonitrile</strong> C1-1e (300 mg, 2.09 mmol) to a single-necked flaskMethanol (50 mL), nickel chloride (543 mg, 4.19 mmol), sodium borohydride (159 mg, 4.19 mmol) was slowly added, and the mixture was reacted at room temperature for 2 hours. The mixture was filtered through diatomaceous earth,It was washed with methanol, and the filtrate was concentrated under reduced pressure to obtain a crude product. The crude product was purified on silica gel(Dichloromethane: methanol = 10: 1) to obtain benzofuran-4-ylmethylamine C2-1(50 mg, 16.2% yield) as a yellow solid.
 

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