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Chemical Structure| 1174632-70-2 Chemical Structure| 1174632-70-2

Structure of 1174632-70-2

Chemical Structure| 1174632-70-2

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Product Details of [ 1174632-70-2 ]

CAS No. :1174632-70-2
Formula : C8H5BrF2O2
M.W : 251.02
SMILES Code : O=C(O)C1=CC=C(CBr)C(F)=C1F
MDL No. :MFCD30538226

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Application In Synthesis of [ 1174632-70-2 ]

* 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 [ 1174632-70-2 ]

[ 1174632-70-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 261763-37-5 ]
  • [ 1174632-70-2 ]
YieldReaction ConditionsOperation in experiment
44.8% With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at 90℃; 2,3-Difluoro-4-methylbenzoic acid (18 g, 105 mmol) and NBS (18.61 g, 105 mmol) were added to a round bottom flask with CC14 (550mL). AIBN (0.086 g, 0.523 mmol) was added and the reaction was heated to reflux (90 C) and stirred at this temperature overnight. The next day, the reaction was cooled to room temperature. The resulting mixture was filtered and washed with DCM. The filtrate was concentrated, diluted with DCM (200 mL) and then extracted with H20 (200 mL). The organic layers were combined, dried, and concentrated to give the title compound (23.5 g, 44.8%). Exact mass calculated for C8H5BrF202: 249.9, found: LCMS m/z = 250.2 [M+H]+; 1H NMR (400 MHz, DMSO-d6) delta ppm 4.76 (s, 2H), 7.42-7.48 (m, 1H), 7.64-7.70 (m, 1H).
44.8% With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at 90℃; 2,3-Difluoro-4-methylbenzoic acid (18 g, 105 mmol) and NBS (18.61 g, 105 mmol) were added to a round bottom flask with CCI4 (550mL). AIBN (0.086 g, 0.523 mmol) was added and the reaction was heated to reflux (90 C) and stirred at this temperature overnight. The next day, the reaction was cooled to room temperature. The resulting mixture was filtered and washed with DCM. The filtrate was concentrated, diluted with DCM (200 mL) and then extracted with H20 (200 mL). The organic layers were combined, dried, and concentrated to give the title compound (23.5 g, 44.8%). Exact mass calculated for C8H5BrF202: 249.9, found: LCMS m/z = 250.2 [M+H]+; NMR (400 MHz, DMSO- 6) delta ppm 4.76 (s, 2H), 7.42-7.48 (m, 1H), 7.64-7.70 (m, 1H).
25.2% With N-Bromosuccinimide; 2,2'-azobis(isobutyronitrile); In tetrachloromethane; at 90 - 100℃; for 3.0h; <strong>[261763-37-5]4-methyl-2,3-difluorobenzoic acid</strong> ((1.724 g, 6.869 mmol) was dissolved in carbon tetrachloride (10 mL),Then N-bromosuccinimide (1.189 g, 6.682 mmol) and azobisisobutyronitrile (43.9 mg, 0.267 mmol) were added.The reaction solution was heated to 90 C for 30 minutes, and then heated to 100 C for 2.5 hours. After the reaction was completed, the reaction solution was cooled to 0 C to precipitate. The precipitate was suction filtered, and the filter cake was washed with n-hexane and water to obtain a crude product. The crude product was dissolved in ethyl acetate (5 mL), n-hexane (10 mL) was added, and a solid was precipitated. Suction filtration and drying under reduced pressure gave 4- (bromomethyl) -2,3-difluorobenzoic acid (627.5 mg, 3.599 mmol, yield 25.2%) as a pale yellow solid.
 

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