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Chemical Structure| 14442-12-7 Chemical Structure| 14442-12-7

Structure of 14442-12-7

Chemical Structure| 14442-12-7

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Product Details of [ 14442-12-7 ]

CAS No. :14442-12-7
Formula : C10H7NO3
M.W : 189.17
SMILES Code : OC(=O)C1=CC(=NO1)C1=CC=CC=C1
MDL No. :MFCD01936010
InChI Key :YGTFDJRCCBKLDM-UHFFFAOYSA-N
Pubchem ID :737474

Safety of [ 14442-12-7 ]

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

Application In Synthesis of [ 14442-12-7 ]

* 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 [ 14442-12-7 ]

[ 14442-12-7 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 72418-40-7 ]
  • [ 90924-12-2 ]
  • [ 14442-12-7 ]
  • 2
  • [ 90924-12-2 ]
  • [ 14442-12-7 ]
YieldReaction ConditionsOperation in experiment
93% With Jones reagent; In acetone; at 20℃; for 3h; To a stirred solution of 8 (12 mg, 0.07 mmol) in acetone (0.4 ml) was added Jones? reagent (50 mul)at room temperature. Then, the mixture was stirred for 3 h. Then water (2 ml) was added, and theaqueous layer was extracted by diethyl ether (5 ml × 3). The organic layer was collected, washedwith water (5 ml × 3), dried over Na2SO4 and concentrated. The residue was recrystallized in CHCl3to afford the product (2a) as white solid (12 mg, 93.0 %).
69% With Jones reagent; In acetone; at 0℃; for 0.5h; Jones reagent 8 N (0.3 mmol) was added dropwise to a solutionof compound 7 (0.1 mmol) in acetone (4 mL) in an ice bath. Thesolution was stirred for 30 min when TLC analysis showed the totalconsumption of the starting material. The solution was diluted inacetone (15 mL) filtered through celite and evapored under vacuum.The crude extract was purified by flash column chromatographyon silica (hexane:ethyl acetate 3:7) affording compound 23 as a white solid. Yield: 69%. Mp: 155.0-57.4 C. 1H NMR (300 MHz,CDCl3): delta = 7.78-7.90 (m, 2H, Ar), 7.45-7.55 (m, 3H, Ar), 7.25 (s, 1H,Isoxazole). 13C NMR (75 MHz, CDCl3): delta =166.9, 165.5, 162.3, 134.4,133.0, 132.8, 131.9, 130.7, 111.3. HRMS (ESI-TOF) m/z: [M- H]- Calcdfor C10H6NO3 188.0353; Found 188.0321.
  • 3
  • [ 1081-30-7 ]
  • [ 14442-12-7 ]
YieldReaction ConditionsOperation in experiment
80% To a stirred solution of alkyl ester (1 equivalent) in dioxane was added aqueous NaOH (1N, 1.5 to 10 equivalents). This mixture was stirred until TLC analysis indicated completion of the reaction (usually 30 mins to 16 h) at which time the reaction was extracted with ether. The resulting aqueous layer was separated, acidified by additional of 1N HCl to pH 4. If there was a formation of solid, the solid was filtered, washed with water and air dried to obtain pure acid. Otherwise, the acidified aqueous layer was extracted with EtOAc, the organic layer was dried over Na2SO4, concentrated under reduced pressure to yield pure acid; 3-Phenylisoxazole-5-carboxylic acid was prepared from 3-phenylisoxazole-5-carboxylic acid methyl ester according to Method C in 80% yield using LiOH as a base and 1:1 mixture of MEOH:THF as a solvent.
2.2 g With sodium hydroxide; In 1,4-dioxane; at 25℃; for 2h; To a stirred solution of methyl 3-phenylisoxazole-5- carboxylate (4.5g, 19.80mmol) in l,4-dioxane(40mL) was added I aOH (21.12mL) added drop wise at 0C. The reaction mixture was stirred for 2h at 25C. Dioxane was distilled off and the crude mixture was diluted with water (20mL) and acidified using IN HC1 (25mL).The resulting precipitate was filtered, washed with water and dried under vacuum to obtain 3-phenylisoxazole-5-carboxylic acid (2.2g).
  • 4
  • [ 908094-01-9 ]
  • [ 14442-12-7 ]
  • [ 1081-30-7 ]
  • 5
  • [ 67-56-1 ]
  • [ 14442-12-7 ]
  • [ 1081-30-7 ]
YieldReaction ConditionsOperation in experiment
94% To a 50-mL round-bottom flask was placed a solution of 3-phen I- l ,2-oxazole-5-carboxylic acid (1.89 g, 9.99 mmol, 1.00 equiv) in DCM (20 mL) then oxalyl chloride (1.9 g, 14.97 mmol, 1.50 equiv) and a drop of DMF were added. The resulting solution was stirred for 1 h at RT then MeOH (5 mL) was added. The reaction was stirred for 1 h at RT then concentrated under reduced pressure affording 1.9 g (94%) of methyl 3-phenyl-l,2-oxazole-5-carboxylate as a yellow solid.
94% To a 50-mL round-bottom flask was placed a solution of 3-phenyl-1,2-oxazole-5-carboxylic acid (1.89 g, 9.99 mmol, 1.00 equiv) in DCM (20 mL) then oxalyl chloride (1.9 g, 14.97 mmol, 1.50 equiv) and a drop of DMF were added. The resulting solution was stirred for 1 h at RT then MeOH (5 mL) wasadded. The reaction was stirred for 1 h at RT then concentrated under reduced pressure affording 1.9 g (94%) of methyl 3-phenyl-1 ,2-oxazole-5-carboxylate as a yellow solid.
  • 6
  • [ 14442-12-7 ]
  • [ 33513-42-7 ]
  • [ 1081-30-7 ]
YieldReaction ConditionsOperation in experiment
94% With oxalyl dichloride; In dichloromethane; at 20℃; for 1h; To a 50-mL round-bottom flask was placed a solution of 3-phenyl-1,2-oxazole-5-carboxylic acid (1.89 g, 9.99 mmol, 1.00 equiv) in DCM (20 mL) then oxalyl chloride (1.9 g, 14.97 mmol, 1.50 equiv) and a drop of DMF were added. The resulting solution was stirred for 1 h at RT then MeOH (5 mL) was added. The reaction was stirred for 1 h at RT then concentrated under reduced pressureaffording 1.9 g (94%) of methyl 3-phenyl-1,2-oxazole-5-carboxylate as a yellow solid.
 

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