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[ CAS No. 1159251-58-7 ] {[proInfo.proName]}

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Chemical Structure| 1159251-58-7
Chemical Structure| 1159251-58-7
Structure of 1159251-58-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 1159251-58-7 ]

CAS No. :1159251-58-7 MDL No. :MFCD19348058
Formula : C10H10N2O2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 190.20 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 1159251-58-7 ]

* 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 [ 1159251-58-7 ]

[ 1159251-58-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 73781-91-6 ]
  • [ 1159251-58-7 ]
  • [ 1159600-88-0 ]
YieldReaction ConditionsOperation in experiment
97% A solution of (5-methyl-3-pyridin-4-yl-isoxazol-4-yl)-methanol (1.00 g, 5.26 mmol) in THF (15 mL) was cooled to 0° C. and sodium hydride (55percent dispersion in mineral oil, 252 mg, 5.78 mmol) was added carefully under an atmosphere of nitrogen. After the resulting suspension was stirred for 0.5 h at ambient temperature methyl 6-chloronicotinate (1.08 g, 6.31 mmol) was added and the suspension was stirred for 18 h at this temperature.The reaction mixture was treated with a aqueous sodium hydroxide (1 N, 15.8 mL, 15.8 mmol) and stirred for 0.5 h at 70° C. The solution was cooled to ambient temperature, diluted with water (15 mL) and washed with tert-butylmethylether (15 mL). The organic layers were extracted with water (20 mL) and the combined aqueous layers were acified to pH=4 with a aqueous hydrochloric acid (25 percent). After the resulting suspension was stirred for 0.5 h at ambient temperature it was filtered off and washed with water (20 mL) affording the title compound (1.60 g, 97percent) which was obtained as a white solid MS: m/e=310.2 [M+H]+.
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