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[ CAS No. 122433-41-4 ] {[proInfo.proName]}

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Chemical Structure| 122433-41-4
Chemical Structure| 122433-41-4
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Product Details of [ 122433-41-4 ]

CAS No. :122433-41-4 MDL No. :MFCD08064227
Formula : C8H8BrNO3 Boiling Point : -
Linear Structure Formula :- InChI Key :OLQOVEOEHQDKSC-UHFFFAOYSA-N
M.W : 246.06 Pubchem ID :14371729
Synonyms :

Safety of [ 122433-41-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P305+P351+P338 UN#:N/A
Hazard Statements:H319 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 122433-41-4 ]

* 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.

  • Upstream synthesis route of [ 122433-41-4 ]

[ 122433-41-4 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 122433-41-4 ]
  • [ 73183-34-3 ]
  • [ 1083168-93-7 ]
YieldReaction ConditionsOperation in experiment
15% With potassium acetate In N,N-dimethyl-formamide at 80℃; AH. Methyl 2-methoxy-5-(4 A5,5-tetramethyl- 1 ,3 ,2-dioxaborolan-2- <n="105"/>vDnicotinate; To a dry flask was added methyl 5-bromo-2-methoxynicotinate (0.5 g, 2.0 mmol), 4,4,4',4',5,5,5',5'-octamethyl-2,2'-bi(l,3,2-dioxaborolane) (0.61 g, 2.4 mmol), and Pd(dppf)Cl2 (82 mg, 0.10 mmol). Potassium acetate (0.6 g, 6.0 mmol) was weighed directly into the flask. The flask was then evacuated and back filled with N2. Anhydrous N,N- dimethylformamide (10.0 mL) was added and the reaction was heated at 80 0C in an oil bath overnight. The reaction mixture was evaporated to dryness. The residue was dissolved in ethyl acetate (10 mL) and washed with water (1OmL). The organics were dried over sodium sulfate and evaporated to dryness. The resulting material was purified by silica gel chromatography (eluting with 0-70percent ethyl acetate in hexanes) to yield the product (0.36 g, 72percent). ESI-MS m/z calc. 249.11, found 250.3 (MW+1)+. Retention time 1.84 minutes.
Reference: [1] Patent: WO2008/141119, 2008, A2, . Location in patent: Page/Page column 104
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