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Chemical Structure| 76008-75-8 Chemical Structure| 76008-75-8

Structure of 76008-75-8

Chemical Structure| 76008-75-8

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Product Details of [ 76008-75-8 ]

CAS No. :76008-75-8
Formula : C9H8BrClO2
M.W : 263.52
SMILES Code : CCOC(=O)C1=CC(Br)=C(Cl)C=C1
MDL No. :MFCD09751942

Safety of [ 76008-75-8 ]

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 [ 76008-75-8 ]

* 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 [ 76008-75-8 ]

[ 76008-75-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 64-17-5 ]
  • [ 42860-10-6 ]
  • [ 76008-75-8 ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; In 1,4-dioxane; for 24h;Heating / reflux; Example 9A. 3-Bromo-4-chlorobenzoic acid ethyl ester.To a solution of <strong>[42860-10-6]3-bromo-4-chlorobenzoic acid</strong> (5.0 g, 21 mmol) in 150 mL absolute ethanol was added 15 mL of 4N HCl/dioxane. The mixture was heated to reflux for 24 hours then cooled to ambient temperature and concentrated under reduced pressure. The residue was partitioned between ethyl acetate and H2O, and the separated organic phase was washed sequentially with saturated NaHCpsi3 solution, brine, dried (Na2SO-O, filtered and concentrated under reduced pressure to provide the title compound. 1H NMR (DMSO-ddelta) delta 8.22 (d, IH), 7.94 (dd, IH), 7.80 (d, IH), 4.33 (q, 2H), 1.33 (t, 3H); MS (DCI4) m/z 263 (M+H)+.
  • 2
  • [ 42860-10-6 ]
  • [ 75-03-6 ]
  • [ 76008-75-8 ]
YieldReaction ConditionsOperation in experiment
97% With caesium carbonate; In hexane; ethyl acetate; acetonitrile; a. Ethyl <strong>[42860-10-6]3-bromo-4-chlorobenzoate</strong>. To a solution of <strong>[42860-10-6]3-bromo-4-chlorobenzoic acid</strong> (3.00 g, 12.74 mmol) and cesium carbonate (6.23 g, 19.11 mmol) in acetonitrile (70 mL) was added iodoethane (5.1 mL, 63.7 mmol). The reaction mixture was heated at reflux overnight. After cooling to room temperature, the solution was extracted with ethyl acetate. The organic layer was washed successively with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated. Choromatography on silica gel (biotage, 5percent EtOAc in hexane) afforded 3.5 g of ethyl <strong>[42860-10-6]3-bromo-4-chlorobenzoate</strong> (97percent). 1H NMR (300 MHz; CDCl3) delta1.40 (t, 3H); 4.37 (q, 2H); 7.52 (d, J=8.1 Hz, 1H); 7.91 (dd, J1=8.4 Hz, J2=1.8 Hz, 1H); 8.28 (d, J=1.8 Hz, 1H).
97% With caesium carbonate; In hexane; ethyl acetate; acetonitrile; a. Ethyl <strong>[42860-10-6]3-bromo-4-chlorobenzoate</strong> To a solution of <strong>[42860-10-6]3-bromo-4-chlorobenzoic acid</strong> (3.00 g, 12.74 mmol) and cesium carbonate (6.23 g, 19.11 mmol) in acetonitrile (70 mL) was added iodoethane (5.1 mL, 63.7 mmol). The reaction mixture was heated at reflux overnight. After cooling to room temperature, the solution was extracted with ethyl acetate. The organic layer was washed successively with water and brine, dried over anhydrous magnesium sulfate, filtered and evaporated. Choromatography on silica gel (biotage, 5percent EtOAc in hexane) afforded 3.5 g of ethyl <strong>[42860-10-6]3-bromo-4-chlorobenzoate</strong> (97percent). 1H NMR (300 MHz; CDCl3) 1.40 (t, 3H); 4.37 (q, 2H); 7.52 (d, J=8.1 Hz, 1H); 7.91 (dd, J1=8.4 Hz, J2=1.8 Hz, 1H); 8.28 (d, J=1.8 Hz, 1H).
 

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