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Chemical Structure| 1223434-16-9 Chemical Structure| 1223434-16-9

Structure of 1223434-16-9

Chemical Structure| 1223434-16-9

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Product Details of [ 1223434-16-9 ]

CAS No. :1223434-16-9
Formula : C8H4BrNO2
M.W : 226.03
SMILES Code : O=C(O)C1=CC=C(Br)C=C1C#N
MDL No. :MFCD18390738

Safety of [ 1223434-16-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 1223434-16-9 ]

* 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 [ 1223434-16-9 ]

[ 1223434-16-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1223434-15-8 ]
  • [ 1223434-16-9 ]
YieldReaction ConditionsOperation in experiment
7.97 g [0366] Preparation Example 76: Preparation of 4-bromo-2-cyanobenzoic acid[0367][0368] Methyl 4-bromo-2-cyanobenzoate (8.53 g) described in Preparation Example 75 was dissolved in dimethoxyethane(140 mL), a solution of lithium hydroxide 1 hydrate (2.24 g) in water (54 mL) was added dropwise underice-cooling, and the mixture was stirred at the same temperature for 30 min. To the reaction mixture was added dropwise1N hydrochloric acid (60 mL) under ice-cooling, saturated brine was added, and the mixture was extracted with ethylacetate. The organic layer was washed with saturated brine, dried over sodium sulfate, and the solvent was evaporatedto give the title compound (7.97 g).MS (ESI) m/z:226(M+H)+
808 mg With water; lithium hydroxide; In methanol; at 20℃; for 4h; A mixture of Compound II (980 mg), 2N aqueous lithium hydroxide solution (6.1 mL) and methanol (18 mL) was stirred at room temperature for 4 hours. The reaction mixture was concentrated under reduced pressure, and to the residue was added 1N aqueous sodium hydroxide solution, and the mixture was extracted with ethyl acetate. The aqueous layer was acidified with 4N hydrochloric acid, and then extracted with chloroform. The chloroform layer was dried over sodium sulfate, and then concentrated under reduced pressure to give Compound III (808 mg).
 

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