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Chemical Structure| 39799-73-0 Chemical Structure| 39799-73-0

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Chemical Structure| 39799-73-0

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Product Details of [ 39799-73-0 ]

CAS No. :39799-73-0
Formula : C15H13NO3
M.W : 255.27
SMILES Code : O=C(OC)C1=CC=C(NC(C2=CC=CC=C2)=O)C=C1
MDL No. :MFCD00032222

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Application In Synthesis of [ 39799-73-0 ]

* 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 [ 39799-73-0 ]

[ 39799-73-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 39799-73-0 ]
  • [ 582-80-9 ]
YieldReaction ConditionsOperation in experiment
94% With lithium hydroxide monohydrate; In tetrahydrofuran; methanol; water; at 20℃; for 17h; b) 4-Benzamidobenzoic acid (A 13) To a solution of methyl 4-benzamidobenzoate A12 (1.00 g, 3.92 mmol) in 4: 1 : 1 v/v THF/MeOH/water (30 mL) was added LiOH H20 (0.505 g, 1 1.8 mmol). The solution was stirred at room temperature for 17 hours and then acidified with 1 M aqueous HCI. The precipitate was collected by filtration to give the title compound (0.886 g, 94percent) as a white solid. H NMR (400 MHz, cf DMSO) delta 10.54 (br s, 1 H), 8.00 - 7.88 (m, 6H), 7.65 - 7.59 (m, 1 H), 7.59 - 7.51 (m, 2H). LCMS-A rt 4.84 min, m/z (positive ion) 242.1 [M+H]+, m/z (negative ion) 240.1 [M-H]\
80% With potassium hydroxide; water; In methanol; for 3h; 20. Og (0. 16MOL) of benzoic acid was dissolved in 250M. OF PYRIDINE and then was cooled in a ice bath of 10C. Thereto, 23. 1g (0. 21MOL) of ethyl CHLOROFORMATE was added dropwise for 30 minutes. The mixture was stirred at room temperature for 2 hours and then filtered to remove salts, to give an anhydride (30.2g, 0. 15MOL). 24. 1G (0. 16MOL) of metyl aminobenzoate was dissolved in 250MQ of pyridine and then was cooled in a ice bath of 10 C. Thereto, the anhydride formed in the previous step was added dropwise for 30 minutes. The mixture was stirred for another 2 hours. After distillation of the solvent, the residue was dissolved in 300MQ of ethyl acetate. The ethyl acetate solution was washed with 5percent hydrochloric acid and with distilled water, dried over magnesium sulfate, decolorized with active charcoal, and then filtered. The filtrate was dried under reduced pressure, to give methyl 4- (PHENYLCARBONYLAMINO) benzoate (34.7g, 85percent yield) as a pale yellow solid. Subsequently, 34.7g of methyl 4- (phenylcarbonylamino) benzoate was dissolved in 500MQ of methanol and thereto 50MQ OF 10percent KOH was added. After stirring for 3 hours, the mixture was neutralized with hydrochloric acid and then filtered, to give an acid compound, 4- (phenylcarbonylamino) benzoic acid (26.2g, 80percent yield). 4- (phenylcarbonylamino) benzoic acid formed (24. 1g, 0. 10MOL) was dissolved in 200MQ of pyridine and then was cooled in a ice bath of 10C. Thereto, 22.9g (0. 13MOL) of ethyl CHLOROFORMATE was added dropwise for 30 minutes. The mixture was stirred at room temperature for 2 hours and then filtered to remove salts, to give an anhydride (38. 7g, 0. 12MOL). 6.9g (0. LOMOL) of hydroxylamine hydrochloride was dissolved in LOOM-C of pyridine and then was cooled in a ice bath of 10C. Thereto, the anhydride formed in the previous step was added dropwise for 30 minutes. The mixture was stirred for another 2 hours. After distillation of the solvent, the residue was dissolved in 300MQ of ethyl acetate. The ethyl acetate solution was washed with 5percent hydrochloric acid and with distilled water, dried over magnesium sulfate, decolorized with active charcoal, and then filtered. The filtrate was dried under reduced pressure, to give a final product, N- [4- (N-HYDROXYCARBAMOYL) phenyl] benzamide (16. 6g, 65percent yield) as a pale yellow solid. TLC (in ethyl acetate: hexane = 1: 1); RF= 0. 53 H-NMR (DMSO-d6): 611. 23 (s, 1H), 10.39 (s, 1H), 9.04 (s, 1H), 8.01 (m, 5H), 7.64 (m, 4H).
 

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