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Chemical Structure| 843646-72-0 Chemical Structure| 843646-72-0

Structure of 843646-72-0

Chemical Structure| 843646-72-0

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Product Details of [ 843646-72-0 ]

CAS No. :843646-72-0
Formula : C14H20BNO3
M.W : 261.13
SMILES Code : O=C(N)CC1=CC=CC(B2OC(C)(C)C(C)(C)O2)=C1
MDL No. :MFCD08669540

Safety of [ 843646-72-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H332-H335
Precautionary Statements:P264-P302+P352-P304+P340-P305+P351+P338-P332+P313-P337+P313

Application In Synthesis of [ 843646-72-0 ]

* 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 [ 843646-72-0 ]

[ 843646-72-0 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 60312-83-6 ]
  • [ 73183-34-3 ]
  • [ 843646-72-0 ]
YieldReaction ConditionsOperation in experiment
78% With potassium acetate;dichloro(1,1'-bis(diphenylphosphanyl)ferrocene)palladium(II)*CH2Cl2; 1,1'-bis(diphenylphosphino)ferrocene; In 1,4-dioxane; at 90℃; for 18h;Inert atmosphere; In a Schlenk tube, a mixture of <strong>[60312-83-6]2-(3-bromophenyl)acetamide</strong> (1.0 g, 4.67 mmol), bis(pinacolato)diboron (2.37 g, 9.34 mmol) and potassium acetate (1.38 g, 14 mmol) was dissolved in dioxane (40ml). The mixture was purged (vacuum-argon three times) and [1,1-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)dichloromethane complex (0.19 g, 0.23 mmol) and 1,1'-bis(diphenylphospheno)ferrocene (0.13 g, 0.23 mmol) were added. The mixture was purged again (vacuum-argon three times) and stirred at 90 C for 18 h. The suspension was filtered off and the filtrated diluted with water and extracted three times with ethyl acetate. The combined organic layers were washed with water and brine, and dried over anhydrous sodium sulphate. Solvent was removed in vacuum and the residue was purified by the SP1 automated purification system to give 0.95 g (3.64 mmol) of the desired compound. Yield = 78% HPLC/MS (15 min) retention time 6.28 min. LRMS: m/z 262 (M+1)
65% With potassium acetate;palladium diacetate; In DMF (N,N-dimethyl-formamide); at 80℃; for 12.3333h; A mixture of 2- (3-BROMO-PHENYL)-ACETAMIDE (600 mg, 2.8 MMOL), potassium acetate (63 mg, 0.28 mmol, 0.1 eq), bis (pinacolato) diboron (783 mg, 3.08 mmol, 1.1 eq), in anhydrous DMF was degassed under N2 for 10 min. Then palladium acetate (824 mg, 8.41 mmol, 3 eq) was added, and the mixture degassed an additional 10 min. The reaction was then heated to 80 C for 12 h. The reaction mixture was then poured into ethyl acetate and water. Extracted with ethyl acetate (3 x 20 mL). The combined organic layer was dried with sodium sulfate, filtered through celite pad and concentrated in vacuo. The crude material was used directly to the next step. Yield : (473 mg, 65%). LC-MS (MH+ = 262).
  • 2
  • [ 843646-72-0 ]
  • [ 1159825-25-8 ]
  • 2-(3'-(piperidin-4-yl)-[1,1'-biphenyl]-3-yl)acetamide [ No CAS ]
 

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