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Chemical Structure| 866633-26-3 Chemical Structure| 866633-26-3

Structure of 866633-26-3

Chemical Structure| 866633-26-3

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Product Details of [ 866633-26-3 ]

CAS No. :866633-26-3
Formula : C7H5BF4O3
M.W : 223.92
SMILES Code : OB(C1=CC(F)=CC=C1OC(F)(F)F)O
MDL No. :MFCD22418268

Safety of [ 866633-26-3 ]

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 [ 866633-26-3 ]

* 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 [ 866633-26-3 ]

[ 866633-26-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 866633-25-2 ]
  • [ 866633-26-3 ]
YieldReaction ConditionsOperation in experiment
To a solution of the aryl bromide (from Step 2 above) (5g) in THF (25 mL) was added Isopropylmagnesium chloride (15 mL, 2.0M in THF) at room temperature. After stirring at the ambient for 2 h, B (OiPr)3 added to the reaction and stirred overnight. The reaction was quenched with IN HCl, stirred at room temperature for 30min and extracted with EtOAc. The residue obtained after removal of the solvent in vacuo, was dissolved in 10% KOH, extracted with ether. The aqueous phase was acidified with concentrated HCl and extracted with EtOAc. The organic layer was dried over Na2SO4 and concentrated to give the aryl boronic acid as a white solid. ¹H NMR (CDCl3) : 7.28-7.32 (m, 1H), 7.17-7.22 (m, 2H) MS (ESI): m/e 225 (M+1)+
A solution of isopropylmagnesium bromide (2M solution in tetrahydrofuran) (83 ml, 0.166 mol) was added drop-wise to a stirred solution of 2-(trifluoromethoxy)-5-fluoro- 1 -bromobenzene (Preparation 49, 27.6 g, 0.107 mol) in anhydrous tetrahydrofuran (125 ml) at -1O0C under an atmosphere of nitrogen. The resulting mixture was stirred at room temperature for 2 hours. Tri/sopropyl borate (26.1 g, 0.139 mol) was then added drop-wise at -100C and the resulting mixture was stirred at room temperature for 16 hours. Hydrochloric acid (1 N aqueous solution) (100 ml) was added drop-wise at O0C and the mixture stirred at room temperature for 30 minutes. Ethyl acetate (150 ml) was added and the layers were separated, the aqueous layer was further extracted with ethyl acetate (2 x 150 ml). The organic extracts were combined and concentrated in vacuo. The residue was dissolved in potassium hydroxide (10% aqueous solution) (50 ml) and extracted with diethyl ether (2 x 150 ml). The separated aqueous layer was acidified to pH~4 by addition of hydrochloric acid (1 N aqueous solution) (100 ml) and extracted with ethyl acetate (3 x 150 ml). The combined organic extracts were dried over anhydrous Na2SO4, filtered and evaporated in vacuo to give an off white solid. Purification by preparative HPLC gave the title compound as an off white solid (5.82 g, 24%).1HNMR (cfe-DMSO): 7.23-7.32 (m, 3H), 7.53-7.55 (m, 1 H), 8.36 (br s, 1 H).MS m/z 223 [MH]-
 

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