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Chemical Structure| 958863-32-6 Chemical Structure| 958863-32-6

Structure of 958863-32-6

Chemical Structure| 958863-32-6

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Product Details of [ 958863-32-6 ]

CAS No. :958863-32-6
Formula : C9H9BrN2O
M.W : 241.08
SMILES Code : OCC1=NC2=CC=C(Br)C=C2N1C
MDL No. :MFCD27500721

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Application In Synthesis of [ 958863-32-6 ]

* 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 [ 958863-32-6 ]

[ 958863-32-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 79-14-1 ]
  • [ 337915-79-4 ]
  • [ 958863-32-6 ]
YieldReaction ConditionsOperation in experiment
To a solution of 42 mL of 6N HCI and 63 mL of water, 5-bromo-N1-methylbenzene- 1 ,2-diamine (9.1 g, 45.4 mmol) and glycolic acid (17.2 g, 227.2 mmol) was added sequentially. The mixture was heated to reflux for 2 hours. After cooling down to room temperature, the mixture was neutralized to PH 9 by ammonium hydroxide. Precipitate formed, filtered, rinsed by water and dried by vacuum to yield (6-bromo-1-methyl-1H- benzo[d]imidazol-2-yl)methanol (8.5 g). 400 MHz 1H NMR (CDCI3) delta 7.5 (d, 1 H), 7.46 (m, 1H), 7.35 (dd, 1 H), 4.92 (s, 2H), 4.74(b, 1 H), 3.8 (s, 3H); MS (M+1) 241 , 243
To a solution of 42 ml 6N HCI and 63 ml water, 5-bromo-N1-methylbenzene-1 ,2-diamine (9.1 g, 45.4 mmol) and glycolic acid (17.2 g, 227.2 mmol) was added sequentially. The mixture was heated to reflux for 2 hours. After cooling down to room temperature, the mixture was neutralized to PH 9 by ammonium hydroxide. Precipitate formed, filtered, rinsed by water and dried by vacuum to yield (6-bromo-1-methyl-1 H-benzo[d]imidazol-2-yl)methanol (8.5 g). 400 MHz 1H NMR (CDCI3) delta 7.5 (d, 1 H), 7.46 (m, 1 H), 7.35 (dd, 1 H), 4.92 (s, 2H), 4.74(b, 1H), 3.8 (s, 3H); MS (M+1 ) 241 , 243.
  • 2
  • [ 302800-13-1 ]
  • [ 958863-32-6 ]
 

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