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Chemical Structure| 913835-30-0 Chemical Structure| 913835-30-0

Structure of 913835-30-0

Chemical Structure| 913835-30-0

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Product Details of [ 913835-30-0 ]

CAS No. :913835-30-0
Formula : C8H10BClO3
M.W : 200.43
SMILES Code : CCOC1=CC=C(Cl)C(B(O)O)=C1
MDL No. :MFCD08235081
InChI Key :LIFPTULDIUUUBK-UHFFFAOYSA-N
Pubchem ID :22309461

Safety of [ 913835-30-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P330-P362-P403+P233-P501

Application In Synthesis of [ 913835-30-0 ]

* 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 [ 913835-30-0 ]

[ 913835-30-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5419-55-6 ]
  • 1-chloro-2-iodo-4-ethoxybenzene [ No CAS ]
  • [ 913835-30-0 ]
YieldReaction ConditionsOperation in experiment
59% 21.3. (2-Chloro-5-ethoxyphenyl)boronic acid; Add, dropwise, 5.5 mL (8.8 mmol) of a 1.6N solution of butyllithium in hexane in the space of 30 min to a solution of 2.38 g (8.4 mmol) of 1-chloro-2-iodo-4-ethoxybenzene in 50 mL of anhydrous THF cooled under argon to -78 C. After 2 h at -70 C., add 1.74 g (9.2 mmol) of triisopropyl borate and stir the reaction mixture for 3 h at room temperature, then distribute in 200 mL of EtOAc/HCl aq 5N 1:1 mixture. Wash the organic phase with 50 mL of water, dry over Na2SO4 and concentrate under reduced pressure. Purify the residue obtained by silica gel column chromatography, eluting with a DCM/methanol gradient from 0 to 10% of methanol. After concentration under reduced pressure, we obtain 990 mg of (2-chloro-5-ethoxyphenyl)boronic acid, in the form of oil.Yield=59%
 

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[ 913835-30-0 ]

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