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Chemical Structure| 21908-07-6 Chemical Structure| 21908-07-6

Structure of 21908-07-6

Chemical Structure| 21908-07-6

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Product Details of [ 21908-07-6 ]

CAS No. :21908-07-6
Formula : C9H9NO3
M.W : 179.17
SMILES Code : O=C(OCC)C1=C(C=O)N=CC=C1
MDL No. :MFCD19690522
Boiling Point : No data available
InChI Key :UHTNTHAZMFWQDB-UHFFFAOYSA-N
Pubchem ID :15639417

Safety of [ 21908-07-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H332
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P330-P363-P501

Application In Synthesis of [ 21908-07-6 ]

* 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 [ 21908-07-6 ]

[ 21908-07-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1721-26-2 ]
  • [ 21908-07-6 ]
YieldReaction ConditionsOperation in experiment
50% With selenium(IV) oxide; In 1,4-dioxane; water; Preparation of 3-carboethoxy-2-pyridinecarboxaldehyde: To a stirred solution of <strong>[1721-26-2]ethyl 2-methylnicotinate</strong> (1.657 g, 10.0 mmol) in 1,4-dioxane (10 mL) and water (1 mL) was added selenium dioxide (1.568 g, 14.1 mmol) and the resultant mixture was heated to reflux overnight. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by column chromatography on silica gel (3:1 hexanes/ethyl acetate) and provided the title compound (0.90 g, 50percent) as a yellow oil. 1H NMR (CDCl3) delta 1.41 (t, 3H, J=7.5 Hz), 4.45 (q, 2H; J=7.5 Hz), 7.56 (dd, 1H, J=6.0, 6.0 Hz), 8.11 (dd, 1H, J=6.0, 1.0 Hz), 8.87 (dd, 1H, J=6.0, 1.0 Hz), 10.34 (s, 1H).
With selenium(IV) oxide; In 1,4-dioxane; Step 1 A mixture of 11.3 g (0.069 mol) of 2-methyl-nicotinic acid ethyl ester and 8.4 g (0.076 mol) of selenium dioxide in 150 mL of dioxane is refluxed under nitrogen for 4 hours. The reaction mixture is cooled to room temperature and filtered. The filtrate is evaporated and the residue is chromatographed on 400 grams of silica gel using 50/50 ethyl acetate/hexanes as the eluant. Appropriate fractions are combined to yield 5 g of 2-formyl-nicotinic acid ethyl ester. 1H NMR (CDCl3) delta 10.3 (s, 1H), 8.8 (m, 1H), 8.0 (m, 1H), 7.5 (m, 1H), 4.30 (q, 2H), 1.4 (t, 3H). TLC (7/3 hexanes/ethyl acetate) Rf=0.2.
In 1,4-dioxane; a) Preparation of 2-formylnicotinic acid ethyl ester 16.9 g of 2-methylnicotinic acid ethyl ester, 22.9 g of selenium (IV) oxide and 240 ml dioxane are combined and refluxed overnight under nitrogen. The mixture is cooled to RT, filtered through celite, and evaporated. The resulting red sludge is diluted with ethylacetate, filtered twice through celite and the solvent removed by evaporation under vacuum.
With selenium(IV) oxide; In 1,4-dioxane; EXAMPLE 7 A solution of <strong>[1721-26-2]ethyl 2-methylnicotinate</strong> (2.0 g, 12.12 mmol), selenium dioxide (20.0 g, 18.18 mmol) and dioxane (10 ml) is heated at 135° for 4 hours. The reaction mixture is filtered and the filtrate is concentrated and purified by prep. TLC to give ethyl 2-formylnicotinate.
With selenium(IV) oxide; In 1,4-dioxane; EXAMPLE 16 A solution of <strong>[1721-26-2]ethyl 2-methylnicotinate</strong> (2.0 g, 12.12 mmol), selenium dioxide (20.0 g, 18.18 mmol) and dioxane (10 ml) is heated at 135° for 4 hours. The reaction mixture is filtered and the filtrate is concentrated and purified by prep. TLC to give ethyl 2-formylnicotinate.

 

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