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Chemical Structure| 128923-99-9 Chemical Structure| 128923-99-9

Structure of 128923-99-9

Chemical Structure| 128923-99-9

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Product Details of [ 128923-99-9 ]

CAS No. :128923-99-9
Formula : C13H10BrNO3
M.W : 308.13
SMILES Code : [O-][N+](C1=CC(OCC2=CC=CC=C2)=CC(Br)=C1)=O
MDL No. :MFCD26401632

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Application In Synthesis of [ 128923-99-9 ]

* 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 [ 128923-99-9 ]

[ 128923-99-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 116632-23-6 ]
  • [ 100-39-0 ]
  • [ 128923-99-9 ]
YieldReaction ConditionsOperation in experiment
91% With potassium carbonate; In acetone; at 20℃; for 2h; 3-Benzyloxy-5-bromo-nitrobenzeneTo an ice-cold solution of <strong>[116632-23-6]3-bromo-5-nitro-phenol</strong> (21.0 g, 96.33 mmol) in acetone (420.0 mL) was added K2CO3 (40.0 g, 289.41 mmol) followed by addition of benzyl bromide (17.20 mL, 144.40 mmol). The resulting reaction mixture was stirred at room temperature for 2 h. The reaction mixture was then diluted with water and extracted with EtOAc (3 x 250.0 mL). The combined organics was dried over anhydrous Na2SO4 and concentrated under reduced pressure. The crude was purified over silica gel (100-200 M, 5percent EtOAc-Hexane) to get the desired product (27.0 g, 91percent). 1H-NMR (400 MHz, DMSO-d6): delta 5.13 (s, 2H), 7.35-7.45 (m, 6H), 7.75 (s, 1 H) and 7.98 (s, 1 H).
51% With potassium carbonate; In acetone; for 3h;Reflux; Industry scale; To a solution of <strong>[116632-23-6]3-bromo-5-nitro-phenol</strong> (770 g, 3.53 mol) in acetone (10 L) was added pulverized K2CO3 (2.45 kg, 17.75 mol) in one portion at rt followed by addition of benzyl bromide (632 mL, 5.32 mol) over a period of 30 min. The resulting reaction mixture was stirred for 15 min then heated at reflux for 3 h. After reaction completion (by TLC), the reaction mixture was filtered through celite and the acetone distilled off. The crude residue thus obtained was purified over silica gel (60-120 M) using EtOAc:hexane (5:95) to obtain the desired product (551 g, 51percent).
51% With potassium carbonate; In [(2)H6]acetone; at 20℃; for 3.25h;Reflux; To a solution of ii (770 g, 3.53 mol) in acetone (10 L) was added K2CO3 (2.45 kg, 17.75 mol) at RT followed by benzyl bromide (632 mL, 5.32 mol) over a period of 30 min. The mixture was stirred for 15 min and then heated at reflux for 3 h. The mixture was filtered through celite and the acetone was distilled off. The residue was purified over silica eluting with EtOAc:hexane (5:95) to obtain iii (551 g, 51percent).
 

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