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Chemical Structure| 31656-92-5 Chemical Structure| 31656-92-5

Structure of 31656-92-5

Chemical Structure| 31656-92-5

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Product Details of [ 31656-92-5 ]

CAS No. :31656-92-5
Formula : C7H7N3
M.W : 133.15
SMILES Code : CC1=CC=CC=C1N=[N+]=[N-]
MDL No. :MFCD11650571

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Application In Synthesis of [ 31656-92-5 ]

* 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 [ 31656-92-5 ]

[ 31656-92-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 615-37-2 ]
  • [ 31656-92-5 ]
YieldReaction ConditionsOperation in experiment
75% With sodium azide; copper diacetate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dimethyl sulfoxide; at 95℃; for 5h; 1.0 mmol o-methyl iodobenzene,1.2 mmol sodium azide,0.15 mmol DBUAnd 0.1mmol of copper acetate were sequentially added to a reaction flask equipped with 3mL of dimethyl sulfoxide,The reaction mixture was stirred at 95 C for 5.0 h,TLC was followed until the reaction was complete,A few drops of aqueous ammonia were added to the reaction mixture,Then extracted with ethyl acetate (10 mL × 3),Then washed once with saturated saline,dry,Suction filtration,Remove the solvent,Purification by column chromatography gave the desired product,Yield 75%.
75% With sodium azide; copper(II) acetate monohydrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; In dimethyl sulfoxide; at 95℃; for 5h; General procedure: CAUTION: Azides are potentially explosive and so appropriateprecautions against blast must be taken when preparing, handlingand heating them. Reactions must be carried out on a small scale. A mixture of the aryl iodide (1.0 mmol), sodium azide (1.2 mmol),DBU (0.15 mmol) and Cu(OAc)2·H2O (0.1 mmol) in DMSO (3.0 mL)in a 10 mL flask was heated to 95 C (the temperature in the reaction flask was monitored) for 1.5-5.0 h. After the reaction was completed asjudged by TLC, the cooled mixture was poured into water (30 mL)containing several drops of ammonia. The resulting aqueous phase was extracted with ethyl acetate (3 × 30 mL). The combined organic phases were washed with brine (50 mL), dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was loaded on asilica gel column and eluted with petroleum ether (boiling range 60-90 C)/ethyl acetate to afford the product.
82%Chromat. With sodium azide; bis(2,2,6,6-tetramethyl-3,5-heptanedionato)copper(II); In N,N-dimethyl-formamide; at 100℃; for 12h;Sealed tube; General procedure: In a 10-mL sealed tube with a spin bar, halobenzene (1 mmol) was used, or in 25-ml round-bottom flask with a spin bar equipped with condenser, boronic acid (1 mmol), was used and DMF (4 ml), sodium azide (1.2 mmol), and Cu(TMHD)2 (0.20 mmol) were added and containers were sealed properly. The reaction mixturewas heated at the 100 C with stirring for desired time and cooled to room temperatureon completion of the reaction. Then the mixture poured into 15 ml of ice-coldwater and extracted with diethyl ether (310 ml). The residue obtained was purifiedby column chromatography (silica gel, 60:20 mesh; petroleum ether = ethyl acetate98:2%) to afford the desired azide products. The organic solution was analyzed by GC and confirmed by GCMS and NMR. The purity of compounds was determinedby GC-MS analysis. All products are known in the literature.
 

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