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Chemical Structure| 886853-92-5 Chemical Structure| 886853-92-5

Structure of 886853-92-5

Chemical Structure| 886853-92-5

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Product Details of [ 886853-92-5 ]

CAS No. :886853-92-5
Formula : C10H7Br2NO4
M.W : 364.97
SMILES Code : O=C(OC)C1=CC=C([N+]([O-])=O)C(C=C(Br)Br)=C1

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Application In Synthesis of [ 886853-92-5 ]

* 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 [ 886853-92-5 ]

[ 886853-92-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 558-13-4 ]
  • [ 148625-35-8 ]
  • [ 886853-92-5 ]
YieldReaction ConditionsOperation in experiment
95.5% With triphenylphosphine; In dichloromethane; at 0℃; for 1h; [00173] To a solution methyl 3-fontauiyl-4-nitrobenzoate (3.137 g, 15 mmol) and CBr4 (5.48 g, 16.5 mmol) in DCM (50 mL) was dropwise added PPh3 (7.86 g, 30 mmol) solution in DCM (50 mL) at 0 0C. After addition, the mixture was stirred for 1 h and warmed to rt. The solution was filtered through a short silica gel coumn, eluted with 20percent EtOAc/hexanes. The solvent was evaporated and the residue was chromotagraphed with 10 to 20percent EtOAc/hexanes to afford the product as a slightly yellow compound (5.23 g, 95.5percent). 1H NMR (400 MHz, CDCl3) delta 8.27 (IH, t, J= 0.8 Hz), 8.19-8.13 (2H, m), 7.76 (IH, s), 3.99 (3H5 s).13C NMR (100 MHz, CDCl3) delta 164.9, 149.4, 134.7, 133.2, 133.1, 131.7, 130.6, 125.2, 94.9, 53.2. HRMS calc'd for C10H8NO4Br2 ([M]+) 363.8820. Found: 363.8823.
74% With triphenylphosphine; In dichloromethane; at 0℃; for 1h;Inert atmosphere; Step 1: Synthesis of methyl 3-(2,2-dibromovinyl)-4-nitrobenzoate (1) (ref. Journal of Organic Chemistry (2007), 72(4), 1341-1346) To a solution of <strong>[148625-35-8]methyl 3-formyl-4-nitrobenzoate</strong> (23.7 mmol) and carbontetrabromide (8.66 g, 26.1 mmol) in dichloromethane (50 ml) was added dropwise a solution of triphenylphosphine (12.44 g, 47.5 mmol) in dichloromethane (50 ml) at 0° C. under a nitrogen atmosphere. The reaction was stirred for 1 h at 0° C. and then allowed to warm to room temperature. A small amount of white solid was formed. The solution was concentrated to 30 mL and then filtered. The organic solvent was concentrated under reduced pressure. The crude product was purified by flash column chromatography (SiO2, 10percent EtOAc in hexanes as eluent) to afford methyl 3-(2,2-dibromovinyl)-4-nitrobenzoate was obtained as a light tan solid (32 g, 74percent); 400 M Hz 1H NMR (CDCl3) 8.26 (br s, 1H), 8.12-8.18 (m, 2H), 7.75 (s, 1H), 3.98 (s, 3H).
With triphenylphosphine; In dichloromethane; at 0℃; 1-(2,2-dibromovinyl)-2-nitrobenzene: 2-nitrobenzaldehyde (10.00 g, 66.2 mmol) was dissolved in DCM (350 mL). CBr4 (23.04 g, 69.5 mmol) was added and the solution cooled to 0 °C in an ice bath. PPh3 (36.4 g, 139 mmol) was added in several portions, and the solution stirred at 0 °C until the reaction was complete by TLC (30 minutes). Hexanes (350 mL) were added to precipitate P(O)Ph3 and P(O)Br2Ph3, and the solution was vacuum filtered over a pad of silica gel, rinsing with 10percent EtOAc (hexanes). The filtrate was collected and solvent removed to yield pure 1-(2,2-dibromovinyl)-2-nitrobenzene (19.80 g, 97percent).
 

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