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Chemical Structure| 607373-82-0 Chemical Structure| 607373-82-0
Chemical Structure| 607373-82-0

4-Methoxy-5-nitropyridin-2(1H)-one

CAS No.: 607373-82-0

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Cat. No.: A194983 Purity: 95%

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Product Details of [ 607373-82-0 ]

CAS No. :607373-82-0
Formula : C6H6N2O4
M.W : 170.12
SMILES Code : COC1=CC(=O)NC=C1[N+]([O-])=O
MDL No. :MFCD07367779
InChI Key :BBXOGUKAXIFZAE-UHFFFAOYSA-N
Pubchem ID :26370134

Safety of [ 607373-82-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis [ 607373-82-0 ]

* 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 [ 607373-82-0 ]

[ 607373-82-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 31872-62-5 ]
  • [ 607373-82-0 ]
YieldReaction ConditionsOperation in experiment
70% Into a 1 L flask containing 250 ml_ of dry THF cooled to -78°C was condensed NH3 (100-150 ml_). Solid t-BuOK (200 mmole, 22.5 g) was added to the THF and was completely dissolved after 10 min of vigorous stirring. In a separate 500 ml_ flask, 10OmL of dry THF containing <strong>[31872-62-5]4-methoxy-3-nitropyridine</strong> (12.3 g, 80 mmole) was cooled to 00C. To this solution was added t-BuOOH (88 mmole, 16 ml_). The t-BuOOH/THF solution was then added to the -78°C ammonia >solution over 20 min via dropping funnel. The reaction solution was allowed to warm to -400C and then stirred at this temperature for 1 h. The reaction was quenched with saturated NH4CI solution (20 mL) and the cooling bath removed. The reaction solution was allowed to stir overnight at RT. The precipitate was filtered and dried under vacuum to give (9.5 g, 70percent) of product as a tan solid: LC/MS: m/z 171 [M+H]+, single component.
51% With tert.-butylhydroperoxide; potassium tert-butylate; ammonia; In tetrahydrofuran; decane; at -78 - 0℃; for 3.16667h; Step 1. 2-Hydroxy-4-methoxy-5-nitropyridine THF (100 mL) was cooled to-78 °C and anhydrous NH3 (-200 mL) was condensed into the THF. Potassium t-butoxid (45.5 g, 405 mmol) was added and the mixture was allowed to warm to--35 °C. <strong>[31872-62-5]4-Methoxy-3-nitropyridine</strong> (25.0 g, 162 mmol) was cooled to 0 °C in THF (200 mL) and a solution of t-BuOOH (5 M in decane, 34 mL, 170 mmol) was added over 10 min. This solution was then added dropwise to the KOt-Bu solution over 1 h, then stirred for 2 h at-35 °C and then carefully quenched with-50 mL of sat. NH4C1 solution. The mixture was allowed to vent and warm to rt overnight, then the organics were concentrated and the residue made acidic with NH4C1 solution and filtered. The solid was washed with cold H20 and dried to give the title compound as a tan solid (14.0 g, 51percent).
90 g With tert.-butylhydroperoxide; potassium tert-butylate; ammonia; In tetrahydrofuran; at -30 - -25℃; for 1h; Example 1 Preparation of 2-hydroxy-4-methoxy-5-nitro pyridine(4-methoxy-5-nitropyridin-2-ol) Charged ammonia gas at -70° C. to a solution of THF (1800 ml). After achieving 1.0 Kg, stopped the gas flow. Charged potassium tert butoxide (182 gms). Temperature was raised to -30° C., charged a solution of <strong>[31872-62-5]4-methoxy-3-nitro pyridine</strong> (100 g) dissolved in THF (250 ml) and tert butyl hydro peroxide (144 ml) to the above mixture at -30 to -25° C. After addition, continued the reaction for 1.0 hr. Saturated ammonium chloride solution (450 ml) was cautiously added and the mixture was allowed to warm to room temperature. The ammonia was evaporated and the residue diluted with water (500 mL). The resulting solid was collected, washed with water and dried to give 2-hydroxy-4-methoxy-5-nitro pyridine(4-methoxy-5-nitropyridin-2-ol) (90.0 g).
 

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