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Chemical Structure| 77823-55-3 Chemical Structure| 77823-55-3

Structure of 77823-55-3

Chemical Structure| 77823-55-3

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Product Details of [ 77823-55-3 ]

CAS No. :77823-55-3
Formula : C7H3Br2ClO2
M.W : 314.36
SMILES Code : O=C(Cl)C1=CC(Br)=C(O)C(Br)=C1

Safety of [ 77823-55-3 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H301-H311-H314-H331
Precautionary Statements:P260-P264-P280-P301+P330+P331+P310-P303+P361+P353+P310+P363-P304+P340+P310-P305+P351+P338+P310-P405-P501
Class:6.1(8)
UN#:2928
Packing Group:

Application In Synthesis of [ 77823-55-3 ]

* 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 [ 77823-55-3 ]

[ 77823-55-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3337-62-0 ]
  • [ 77823-55-3 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; for 6h;Heating / reflux; <strong>[3337-62-0]3,5-Dibromo-4-hydroxybenzoic acid</strong> (5.1 g, 17.23 mmol) was refluxed in thionyl chloride (100 mL) for 6h. The reaction mixture was cooled and the excess thionyl chloride removed. The product was used in the next step without further purification. Glycine methyl ester hydrochloride (4. 33 g, 34.5 mmol) was dissolved in dichloromethane (430 mL) and triethyl amine (20 mL, 143.6 mmol). The acid chloride (17.23 mmol) was added in small portions. Stirring was continued overnight. The solvent was evaporated. The reaction mixture was dissolved in dichloromethane and washed with hydrochloric acid (0.1 M aqueous solution). The organic phase was dried over sodium sulphate, filtered and the solvent removed. A small amount of ethyl acetate was added and the mixture was filtered to give 4.21 g (88percent) of almost pure compound. The product was crystallized from heptanes/ethyl acetate to give 2.5 g of the title compound (52percent yield) as a white powder.
With thionyl chloride; for 6h;Heating / reflux; <strong>[3337-62-0]3,5-Dibromo-4-hydroxybenzoic acid</strong> (5.1 g, 17.23 mmol) was refluxed in thionyl chloride (100 mL) for 6 h. The reaction mixture was cooled and the excess thionyl chloride removed. The product was used in the next step without further purification.
With thionyl chloride; In 1,2-dimethoxyethane; at 80℃; Step 1 Production of 3,5-dibromo-4-hydroxybenzoyl chloride 1,2-Dimethoxyethane (20 mL) was added to <strong>[3337-62-0]3,5-dibromo-4-hydroxybenzoic acid</strong> (2.96 g) to dissolve same by heating the mixture to 80° C. Thionyl chloride (1.1 mL) was added, and the mixture was stirred overnight at 80° C. The reaction mixture was concentrated under reduced pressure, azeotroped with toluene, and dried to give the title compound (3.1562 g) as a white solid.
With thionyl chloride; In 1,2-dimethoxyethane; at 80℃; Step 1 Production of 3,5-dibromo-4-hydroxybenzoyl chloride 1,2-Dimethoxyethane (20 mL) was added to <strong>[3337-62-0]3,5-dibromo-4-hydroxybenzoic acid</strong> (2.96 g) to dissolve same by heating the mixture to 80° C. Thionyl chloride (1.1 mL) was added, and the mixture was stirred overnight at 80° C. The reaction mixture was concentrated under reduced pressure, azeotroped with toluene, and dried to give the title compound (3.1562 g) as a white solid.

  • 2
  • [ 110-71-4 ]
  • [ 3337-62-0 ]
  • [ 77823-55-3 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; Step 1 Production of 3,5-dibromo-4-hydroxybenzoyl chloride 1,2-Dimethoxyethane (20 mL) was added to <strong>[3337-62-0]3,5-dibromo-4-hydroxybenzoic acid</strong> (2.96 g) to dissolve same by heating the mixture to 80° C. Thionyl chloride (1.1 mL) was added, and the mixture was stirred overnight at 80° C. The reaction mixture was concentrated under reduced pressure, azeotroped with toluene, and dried to give the title compound (3.1562 g) as a white solid.
 

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