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Chemical Structure| 1231257-90-1 Chemical Structure| 1231257-90-1

Structure of 1231257-90-1

Chemical Structure| 1231257-90-1

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Product Details of [ 1231257-90-1 ]

CAS No. :1231257-90-1
Formula : C15H22BNO3
M.W : 275.15
SMILES Code : CC1(C)C(C)(C)OB(O1)C2=CC(N(C(C)=O)C)=CC=C2
MDL No. :MFCD18383616

Safety of [ 1231257-90-1 ]

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 [ 1231257-90-1 ]

* 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 [ 1231257-90-1 ]

[ 1231257-90-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 480424-93-9 ]
  • [ 74-88-4 ]
  • [ 1231257-90-1 ]
YieldReaction ConditionsOperation in experiment
75% Lambda/-Methyl-N-(3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)acetamide [00294] N-(3-(4,4,5,5-tetramethyl-l,3,2-dioxaborolan-2-yl)phenyl)acetamide (1.0 g, 3.83 mmol) was dissolved in anhydrous THF (32 mL). Sodium hydride (306 mg, 7.66 mmol - 60% in mineral oil) was added and the resulting cloudy white mixture stirred at 2O0C for 30 minutes under an N2 atmosphere. Methyl iodide (716 muL, 11.49 mmol) was added dropwise and the mixture stirred at 2O0C for 16 hours. The reaction mixture was partitioned between EtOAc (100 mL). The aqueous layer was acidified with IM HClaq and re-extracted with EtOAc (100 mL). The organic extracts were combined, dried over MgSO4, and concentrated in vacuo to give a pale yellow oil (1.34 g). Column chromatography (0:1 - 1 :3 EtOAc: petroleum ether gradient) gave the title compound as a clear oil (791 mg, 75%). LCMS RT = 1.95 min MH+ 276.4. 1H NMR (d6-DMSO): 7.63 (IH, s), 7.51 (IH, s), 7.46 (2H, m), 3.15 (3H, s), 1.30 (12H, s), 1.07 (3H, s).
60% N-Methyl-N-(3-(4'.4'.5'.5'-tetramethyl-r.3'.2'-dioxaborolan-2'-vpphenvpacetamide [00257] A solution of N-(3-(4>,4>,5',5'-tetramethyl-r,3>,2>-dioxaborolan-2>- yl)phenyl)acetamide (500 mg, 1.915 mmol) in anhydrous THF (10.0 mL) was transferred via a canula to a mixture of sodium hydride (60% in mineral oil; 153 mg, 3.830 mmol) and anhydrous THF (10.0 mL) under a nitrogen atmosphere and the resulting mixture was stirred at room temperature for 30 minutes. Methyl iodide (0.36 mL, 5.745 mmol) was then added and stirring continued for 16 hours. The reaction mixture was then quenched with ammonium chloride (sat. aq.), followed by extraction into EtOAc. The organic layer was dried (MgSO4), concentrated in vacuo and purified by flash column chromatography (3:1 EtOAc:40-60 petrol) to give the title compound (317 mg, 60%). 1U NMR (d6-DMSO): 7.68- 7.57 (IH, br s), 7.53-7.40 (3H, br m), 3.14 (3H, s), 1.73 (3H, s), 1.30 (12H, s).
 

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