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Chemical Structure| 148928-60-3 Chemical Structure| 148928-60-3

Structure of 148928-60-3

Chemical Structure| 148928-60-3

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Product Details of [ 148928-60-3 ]

CAS No. :148928-60-3
Formula : C7H3F2NO4
M.W : 203.10
SMILES Code : O=[N+](C1=C2OC(F)(F)OC2=CC=C1)[O-]
MDL No. :MFCD29043492

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Application In Synthesis of [ 148928-60-3 ]

* 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 [ 148928-60-3 ]

[ 148928-60-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1583-59-1 ]
  • [ 148928-60-3 ]
YieldReaction ConditionsOperation in experiment
28.57% With sulfuric acid; nitric acid; acetic acid; In acetic anhydride; at 10℃; for 1.5h; In a 1000 ml three-neck bottle,Add 300 ml of acetic anhydride,200 ml of acetic acid,15.8 g (0.1 mol) shown in the formula M-01 2,2-difluorobenzo [d] [1,3] dioxolane,Cool down to 10 C,A mixture of 9.69 g (0.1 mol) of 65% nitric acid and 20.6 g of 98% sulfuric acid was slowly added dropwise.The reaction was incubated at 10 C for 90 minutes.After adding water and dichloromethane, the organic layer was washed with water until neutral, concentrated to dryness, and then separated by silica gel column chromatography, petroleum ether: ethyl acetate = 10:1 (volume ratio).5.8 g of 2,2-difluoro-4-nitrobenzo[d][1,3]dioxane was obtained according to the formula M-02, and the yield was 28.57%.
28.57% With sulfuric acid; nitric acid; In acetic anhydride; acetic acid; at 10℃; for 1.5h; 1000 Ml three-neck bottle in, add 300 ml of acetic anhydride, 200 ml of acetic acid, 15.8 g (0.1 muM) type M - 01 shown and [d] 2, 2 - difluoro [1, 3] the iodine, lowering the temperature to 10 C, slowly dropping 9 . 69 g (0.1 muM) 65% nitric acid and 20.6 g 98% sulfuric acid mixture, [...] 10 C insulation reaction 90 minutes, liquid water and methylene chloride, the organic layer washed to neutral, to dry after concentration, silica gel column chromatography separation, petroleum ether: ethyl acetate=10:1 ([...]) elution, formula M - 02 shown -4 - 2, 2 - difluoro [d] nitrobenzene and [1, 3] the iodine 5.8 g, yield 28.57%.
28.57% With sulfuric acid; nitric acid; acetic anhydride; acetic acid; at 10℃; for 1.5h; In a 1000 ml three-necked flask, add 300 ml of acetic anhydride, 200 ml of acetic acid,15.8 g (0.1 mol) of <strong>[1583-59-1]2,2-difluorobenzo[d][1,3]dioxolane</strong> represented by the formula M-01, cooled to 10 C,A mixture of 9.69 g (0.1 mol) of 65% nitric acid and 20.6 g of 98% sulfuric acid was slowly added dropwise.Add the reaction at 10 C for 90 minutes, add water and dichloromethane, and wash the organic layer to neutral.After concentration to dryness, it was separated by silica gel column chromatography, eluting with petroleum ether: ethyl acetate = 10:1 (volume ratio)5.8 g of 2,2-difluoro-4-nitrobenzo[d][1,3]dioxolane represented by the formula M-02 was obtained in a yield of 28.57%.
 

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