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Chemical Structure| 14300-33-5 Chemical Structure| 14300-33-5

Structure of 14300-33-5

Chemical Structure| 14300-33-5

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Product Details of [ 14300-33-5 ]

CAS No. :14300-33-5
Formula : C7H12O
M.W : 112.17
SMILES Code : OC(C1CC1)C2CC2
MDL No. :MFCD00019249
InChI Key :PIXLZMHERIHLJL-UHFFFAOYSA-N
Pubchem ID :84336

Safety of [ 14300-33-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 14300-33-5 ]

* 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 [ 14300-33-5 ]

[ 14300-33-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 14300-33-5 ]
  • [ 21642-98-8 ]
  • 1-(dicyclopropylmethyl)-4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile [ No CAS ]
YieldReaction ConditionsOperation in experiment
With bis(2-methoxyethyl) azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 35℃; for 15.0h; A) 1-(dicyclopropylmethyl)-<strong>[21642-98-8]4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile</strong> (0739) To a mixture of <strong>[21642-98-8]4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile</strong> (5.0 g), triphenylphosphine (13.1 g), dicyclopropylmethanol (7.47 g) and tetrahydrofuran (100 mL) was added bis(2-methoxyethyl) azodicarboxylate (11.7 g) at 0°C. The reaction mixture was stirred at room temperature for 15 hr. The reaction mixture was added to water, and the mixture was extracted with ethyl acetate. The obtained organic layer was washed with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure and the residue was dissolved in diethyl ether, and triphenylphosphine oxide (5 mg) was added. Insoluble material was filtered off and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/ethyl acetate) to give a crude purification product, which was purified by silica gel column chromatography (basic silica gel, hexane/ethyl acetate) to give a crude title compound (8.80 g). MS (ESI+): [M+H]+ 245.3.
8.80g With azodicarboxylic acid bis(2-methoxyethyl) ester; triphenylphosphine; In tetrahydrofuran; at 0 - 35℃; for 15.0h; <strong>[21642-98-8]4-methoxy-2-oxo-1,2-dihydropyridine-3-carbonitrile</strong> (5.0 g), triphenylphosphine (13.1 g), a mixture of di-cyclopropyl-methanol (7.47 g) and tetrahydrofuran (100 mL), azo dicarboxylic acid bis (2-methoxyethyl) a (11.7 g) was added at 0 ° C.. The reaction mixture was stirred for 15 hours at room temperatureThe reaction mixture was added to water and extracted with ethyl acetate. The resulting organic layer was washed with water then with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was dissolved in diethyl ether, was added triphenyl phosphine oxide (5 mg).The insoluble material was collected by filtration. The filtrate was concentrated under reduced pressure. A silica gel column residueIt was purified by chromatography (hexane / ethyl acetate) and purified by silica gel column chromatography after obtaining a crude product (NH, hexane / ethyl acetate) to give the title compound of crude a (8.80 g).
 

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