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Chemical Structure| 35249-62-8 Chemical Structure| 35249-62-8

Structure of 35249-62-8

Chemical Structure| 35249-62-8

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Product Details of [ 35249-62-8 ]

CAS No. :35249-62-8
Formula : C11H12BrNO2
M.W : 270.12
SMILES Code : N#CCCC1=CC(OC)=C(OC)C=C1Br
MDL No. :MFCD00100650

Safety of [ 35249-62-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 35249-62-8 ]

* 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 [ 35249-62-8 ]

[ 35249-62-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35249-62-8 ]
  • [ 35202-54-1 ]
YieldReaction ConditionsOperation in experiment
80% With n-butyllithium; In tetrahydrofuran; hexane; at -10℃;Inert atmosphere; Example 1.Preparation of 3,4-dimethoxy-bicyclo[4.2.0]octa-l,3,5-triene-7-carbonitrile (III)In a 250 ml flask in argon atmosphere 50 ml of anhydrous tetrahydrofuran was added. The mixture was cooled to -10 °C and 33 ml of 2.5 M butyllithium hexane solution was added 25 dropwise while the temperature was kept below-10 °C. Then the reaction was stirred for 10 minutes at -10°C. 13.0 ml of diisopropylamine (or 10.0 ml diethylamine) was added dropwise while the temperature was kept at -10°C.Then the reaction was stirred for 10 minutes. 10.0 g of 3-(2-bromo-4,5-dimethoxy- phenyl)-propionitrile (II) dissolved in 30 ml of anhydrous tetrahydrofuran was added30 dropwise to the solution at -10 °C. The reaction was stirred at -10 °C.After the reaction had been completed it was allowed to warm up to 0 °C and 100 ml of 1 M hydrochloric acid was added dropwise while the temperature was kept below 20 °C. After 5 minutes stirring the phases were separated. The aqueous phase was washed twice with 50 ml of toluol. The combined organic phases were washed with 1x50 ml of 1 M hydrochloric acid and 1x50 ml of saturated sodium chloride solution.The organic phase was evaporated in vacuum to 20 g. 20 ml of ethanol was added to the residue and it was evaporated in vacuum again to 20 g. 30 ml of ethanol was added to the residue and it was evaporated again to 20 g.The residue was stirred on ice-water. The product was crystallized, it was stirred for 30 minutes at 0-5 °C. Then it was filtered and washed with ethanol. It was dried in vacuum at 40 °C.5.55 g of the title compound was obtained in 80percent yield.
74% With sodium amide; In ammonia; at 20℃; for 2h;liquid NH3; Based on Tetrahedron 1973, 29, pp 73-76 To a solution of NaNH2, prepared starting from 200 mL of liquid NH3 and 1 g of Na (catalyst: FeCl3) there are added, in portions, 5.4 g of 3-(2-bromo-4,5-dimethoxyphenyl)propanenitrile and the reaction mixture is stirred at ambient temperature for 2 hours. After evaporating off the excess NH3, 2 g of NH4Cl and 200 mL of water are added in portions. The grey crystals formed are collected and recrystallised from ethanol to yield 2.38 g of the expected product. Yield=74percent m.p.=84-85° C.
74% With iron(III) chloride; ammonia; sodium; at 20℃; for 2h; EXAMPLE 4 3,4-dimethoxybicyclo[4.2.0]octa-1,3,5-triene-7-carbonitrile Based on Tetrahedron 1973, 29, pp 73-76 To a solution of NaNH2, prepared starting from 200 mL of liquid NH3 and 1 g of Na (catalyst: FeCl3) there are added, in portions, 5.4 g of 3-(2-bromo-4,5-dimethoxyphenyl)propanenitrile and the reaction mixture is stirred at ambient temperature for 2 hours. After evaporating off the excess NH3, 2 g of NH4Cl and 200 mL of water are added in portions. The grey crystals formed are collected and recrystallised from ethanol to yield 2.38 g of the expected product. Yield=74percent m.p.=84-85° C.
74% With sodium amide; at 20℃; for 2h; Based on Tetrahedron 1973, 29, pp 73-76 [0035] To a solution of NaNH2, prepared starting from 200 mL of liquid NH3 and 1 g of Na (catalyst: FeCl3) there are added, in portions, 5.4 g of 3-(2-bromo-4,5-dimethoxyphenyl)propanenitrile and the reaction mixture is stirred at ambient temperature for 2 hours. After evaporating off the excess NH3, 2 g of NH4Cl and 200 mL of water are added in portions. The grey crystals formed are collected and recrystallised from ethanol to yield 2.38 g of the expected product. [0036] Yield=74percent [0037] m.p.=84-85° C.

 

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