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Chemical Structure| 31535-89-4 Chemical Structure| 31535-89-4

Structure of 31535-89-4

Chemical Structure| 31535-89-4

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Product Details of [ 31535-89-4 ]

CAS No. :31535-89-4
Formula : C13H10N2O
M.W : 210.23
SMILES Code : O=C1C=CC2=C(C3=NC=CC=C3C=C2)N1C
MDL No. :MFCD00185681

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Application In Synthesis of [ 31535-89-4 ]

* 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 [ 31535-89-4 ]

[ 31535-89-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 31535-89-4 ]
  • [ 7089-68-1 ]
YieldReaction ConditionsOperation in experiment
75% Reference Example 32-Chloro-1,10-phenanthroline (3) [0113] [Chem. 20] [0114] Under a stream of argon, to compound (2) (8 g; 38 mmol), phosphorus oxychloride (72 mL) and phosphorus pentachloride (9.8 g; 47.6 mmol) were added in an ice bath. The resulting reaction mixture was stirred and refluxed for 8 hours, and excess phosphorus oxychloride was removed under reduced pressure. To the resulting reaction concentrate, ice water and concentrated aqueous ammonia were added and the resulting mixture was made alkaline to precipitate crude crystals. The crude crystals were separated by filtration and washed with water, and then dried under reduced pressure to give 6.1 g (yield: 75percent) of the title compound (3). [0115] 1H NMR (DMSO-d6) d: 7.80-7.88 (m, 2 H), 8.07 (s, 2 H), 8.54 (d, J = 8.5 Hz, 1 H), 8.60 (d, J = 8.5 Hz, 1 H), 9.14 (d, J = 7 Hz, 1 H)
75% Production Example 32-Chloro-1,10-phenanthroline (3)[0149] [Chem. 26] [0150] Under a stream of argon, to compound (2) (8 g; 38 mmol), phosphorus oxychloride (72 mL) and phosphorus pentachloride (9.8 g; 47.6 mmol) were added in an ice bath. The resulting reaction mixture was stirred and refluxed for 8 hours, and excess phosphorus oxychloride was removed under reduced pressure. To the resulting reaction concentrate, ice water and concentrated aqueous ammonia were added and the resulting mixture was made alkaline to precipitate crude crystals. The crude crystals were separated by filtration and washed with water, and then dried under reduced pressure to give 6.1 g (yield: 75percent) of the title compound (3).[0151] 1H NMR (DMSO-d6)d: 7.80-7.88 (m, 2H), 8.07 (s, 2H), 8.54 (d, J=8.5 Hz, 1H), 8.60 (d, J=8.5 Hz, 1H), 9.14 (d, J=7 Hz, 1H)
 

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