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Chemical Structure| 1056456-21-3 Chemical Structure| 1056456-21-3

Structure of 1056456-21-3

Chemical Structure| 1056456-21-3

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Product Details of [ 1056456-21-3 ]

CAS No. :1056456-21-3
Formula : C15H22BNO3
M.W : 275.15
SMILES Code : CC1(C)C(C)(C)OB(O1)C2=CC=C(N(C(C)=O)C)C=C2
MDL No. :MFCD22493726
InChI Key :ZTPFLQNGOULVNC-UHFFFAOYSA-N
Pubchem ID :59232387

Safety of [ 1056456-21-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1056456-21-3 ]

* 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 [ 1056456-21-3 ]

[ 1056456-21-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 214360-60-8 ]
  • [ 74-88-4 ]
  • [ 1056456-21-3 ]
YieldReaction ConditionsOperation in experiment
80% With triethylamine; In tetrahydrofuran; at 20℃; for 4h; <strong>[214360-60-8]N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide</strong> (1.0 g, 3.83 mmol), methyl iodide (1.2 eq.) and triethylamine were dissolved in tetrahydrofuran (10 mL), and the reactants were stirred at room temperature for 4 hours. After completion of the reaction was confirmed by TLC, water (50 mL) and ethyl acetate (500 mL) were added to the reactants, followed by extraction. The organic layer was washed with brine and distilled under reduced pressure. The residue was purified by silica gel column chromatography using ethyl acetate and hexane as a developing solvent, thus affording the title compound N-methyl-<strong>[214360-60-8]N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)acetamide</strong> (14a). Yield: 80%.MS (ESI+) m/z 276.1 (M+1)
80% With triethylamine; In tetrahydrofuran; at 20℃; for 4h; Preparation Example 19: Preparation of N-methyl-N-(4-(4,4,5,5-tetramethyl-l,3,2- <n="64"/>dioxaborolan-2-yl)phenyI)acetamide (14a)N-(4-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)acetamide (1.0 g, 3.83 mmol), methyl iodide (1.2 eq.) and triethylamine were dissolved in tetrahydrofuran (10 mL), and the reactants were stirred at room temperature for 4 hours. After completion of the reaction was confirmed by TLC, water (50 mL) and ethyl acetate (500 mL) were added to the reactants, followed by extraction. The organic layer was washed with brine and distilled under reduced pressure. The residue was purified by silica gel column chromatography using ethyl acetate and hexane as a developing solvent, thus affording the title compound N-methyl-N-(4- (4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)acetamide (14a). Yield: 80%.MS(ESI+) m/z 276.1 (M+1)
 

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