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Chemical Structure| 21962-53-8 Chemical Structure| 21962-53-8

Structure of 21962-53-8

Chemical Structure| 21962-53-8

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Product Details of [ 21962-53-8 ]

CAS No. :21962-53-8
Formula : C9H7NO2
M.W : 161.16
SMILES Code : N#CC1=CC=C(OC)C(C=O)=C1
MDL No. :MFCD13195275
InChI Key :HJDXZGCTGAWUFZ-UHFFFAOYSA-N
Pubchem ID :10241098

Safety of [ 21962-53-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H312-H315-H319-H332-H335
Precautionary Statements:P261-P280-P305+P351+P338

Application In Synthesis of [ 21962-53-8 ]

* 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 [ 21962-53-8 ]

[ 21962-53-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 124-41-4 ]
  • [ 146137-79-3 ]
  • [ 21962-53-8 ]
YieldReaction ConditionsOperation in experiment
59% In methanol; for 2h;Inert atmosphere; Reflux; 3- formyl-4-methox benzonitrile In a 10 mL reactor flask, <strong>[146137-79-3]4-fluoro-3-formylbenzonitrile</strong> (900 mg, 6.04 mmol) was dissolved under argon in 2 mL of methanol. Sodium methoxide (1.232 mL, 6.64 mmol) was added and the reaction mixture was heated at reflux for 2h. TLC showed no more starting material. The reaction mixture was poured into 10 mL of water. The resulting solid was filtered, washed with water, DIPE and dried in vacuo. The residue was purified by flash chromatography, eluted with a gradient from pretroleum ether to MTBE give 587 mg of a grey solid (Yield :59percent) LC-MS: 98percent 1H NMR (300 MHz, DMSO-d6) delta ppm: 10.28 (s, 1H), 8.12 (dd, J = 8.8, 2.2 Hz, 1H), 8.05 (d, J = 2.1 Hz, 1H), 7.43 (d, J = 8.8 Hz, 1H), 4.01 (s, 3H).
  • 2
  • [ 67-56-1 ]
  • [ 146137-79-3 ]
  • [ 21962-53-8 ]
YieldReaction ConditionsOperation in experiment
88% With sodium methylate; at 20℃; To a solution of <strong>[146137-79-3]5-cyano-2-fluorobenzaldehyde</strong> (500?mg, 3.35?mmol) in MeOH (5?mL) was added CH3ONa (362?mg, 6.71?mmol, 2 equiv). The mixture was stirred at rt for 3?h. After the reaction was completed, the product was extracted with EtOAc (20?mL x 3). The organic layers were combined, washed with saturated brine, dried over Na2SO4 and filtered. All volatiles were evaporated in vacuo and the product was obtained after flash chromatography (hexane: EtOAc?=?30: 1) as a white solid (478?mg, 88%), 1H NMR (400?MHz, Chloroform-d) delta 10.44 (s, 1H), 8.13 (s, 1H), 7.84 (d, J?=?8.8?Hz, 1H), 7.12 (d, J?=?8.9?Hz, 1H), 4.04 (s, 3H).
83% With sodium; at 35℃; for 3.5h; Sodium pieces (6 g, 260 mmol) were carefully added to a solution of anhydrous MeOH (200 mL) at 5 C. The reaction mixture was stirred until the sodium was dissolved (~ 15 minutes) then <strong>[146137-79-3]4-fluoro-3-formylbenzonitrile</strong> (30 g, 200 mmol) was added and the mixture was stirred at 35 C for 3.5 h. The reaction mixture was then cooled to room temperature and the suspension collected by filtration. The resulting solid was then recrystallized from EtOAc to afford the title compound (27 g, 83%) as an off-white solid. 1H NMR (400MHz, CDCl3) delta =10.43 (s, 1H), 8.13 (d, J = 2.2 Hz, 1H), 7.83 (dd, J = 8.6, 2.0 Hz, 1H), 7.11 (d, J = 8.8 Hz, 1H), 4.03 (s, 3H).
 

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• Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blaise Reaction • Blanc Chloromethylation • Bucherer-Bergs Reaction • Catalytic Hydrogenation • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • Friedel-Crafts Reaction • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Julia-Kocienski Olefination • Knoevenagel Condensation • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nomenclature of Ethers • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Preparation of Amines • Preparation of Ethers • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Ethers • Reformatsky Reaction • Ritter Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Stetter Reaction • Stobbe Condensation • Tebbe Olefination • Thorpe-Ziegler Reaction • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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