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Chemical Structure| 1024-59-5 Chemical Structure| 1024-59-5

Structure of 1024-59-5

Chemical Structure| 1024-59-5

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Product Details of [ 1024-59-5 ]

CAS No. :1024-59-5
Formula : C10H6F4O4
M.W : 266.15
SMILES Code : O=C(C1C(C(=O)OC)=C(F)C(F)=C(F)C=1F)OC
MDL No. :MFCD00298233

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Application In Synthesis of [ 1024-59-5 ]

* 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 [ 1024-59-5 ]

[ 1024-59-5 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 827-08-7 ]
  • [ 616-38-6 ]
  • [ 1024-59-5 ]
  • 2
  • [ 126-33-0 ]
  • [ 1024-59-5 ]
  • dimethyl 4-t-butylamino-3,5,6-trifluoro-1,2-benezenedicarboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In n-heptane; water; toluene; Method B 3,4,5,6-Tetrafluoro-1,2-benzenedicarboxylic acid, dimethyl ester (Example 1), 13.5 g, is dissolved in a mixture of toluene (10 ml) and tetramethylene sulfone (70 ml) by warming. The solution is cooled to 25 C. Tertiary-butylamine (24.71 g) is added and the solution is stirred at ambient temperature for six hours. Water (100 ml) is added and the solution is extracted with heptanes (3*100 ml). The combined heptane extract is then extracted first with a 5% aqueous solution of hydrochloric acid (100 ml), then with demineralized water (100 ml). The heptane portions are combined and concentrated to give dimethyl 4-t-butylamino-3,5,6-trifluoro-1,2-benezenedicarboxylate as an oil.
  • 3
  • [ 126-33-0 ]
  • [ 34973-43-8 ]
  • [ 1024-59-5 ]
YieldReaction ConditionsOperation in experiment
72% With hydrogenchloride; potassium fluoride; triethylamine; In methanol; n-heptane; water; toluene; Method A Anhydrous potassium fluoride (63 g) and tetramethylenesulfone (85 ml)) are combined and the mixture heated to 150 C. Perchlorophthalide (Example A) (24 g) is added over a 30-minute period. The mixture is then stirred at 150-155 C. for 3.5 hours. It is cooled to 100 C. and toluene (100 ml) is added followed by methanol (4.75 g). The mixture is then cooled to 10 C. and triethylamine (14.95 g) slowly added. The mixture is stirred at 25 C. overnight. The next day it is filtered and the residue washed with toluene (3*100 ml). Heptane (200 ml) is added to the combined toluene filtrate. This solution is extracted with a 5% aqueous solution of hydrochloric acid (3*100 ml) followed by water (3*100 ml). The organic layer is concentrated to a solid (17.6 g), which is recrystallized from toluene (5 ml), and heptanes (15 ml). The crystals are collected and washed with heptanes (2*10 ml) and vacuum dried to give 3,4,5,6-tetrafluoro-1,2-benzenedicarboxylic acid, dimethyl ester (13.6 g, 72%); mp 70-72 C., GC (95.9%).
65% With hydrogenchloride; potassium fluoride; triethylamine; In methanol; water; Method B Anhydrous spray-dried potassium fluoride (63 g) is added to a 500-ml flask followed by tetramethylenesulfone (87 ml). The mixture is heated with stirring to 155 C. Perchlorophthalide (Example A) (24 g) is added in portions over 25 minutes at 145-155 C. The resulting mixture is then stirred at 140-150 C. for three hours and 15 minutes. The mixture is cooled to 10 C. and methanol (4.85 g) is added. Triethylamine (14.95 g) is then added over 20 minutes with ice bath cooling in order to maintain the reaction temperature between 10-20 C. The resulting mixture is allowed to stir overnight at room temperature. The next day it is filtered and the salts washed with toluene (3*100 ml). The combined toluene filtrates are diluted with heptanes (200 ml) and extracted with a 5% aqueous solution of hydrochloric acid (3*75 ml) and then water (2*100 ml). The organic layer is concentrated to a solid (17.0 g). This is recrystallized from toluene (10 ml) and heptanes (10 ml), and after cooling in an ice bath the crystals are collected and washed with heptanes (3*10 ml) and vacuum dried to give 3,4,5,6-tetrafluoro-1,2-benzenedicarboxylic acid, dimethyl ester (12.2 g, 65%); mp 70-72 C., GC (97.2%).
 

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