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Chemical Structure| 113589-26-7 Chemical Structure| 113589-26-7

Structure of 113589-26-7

Chemical Structure| 113589-26-7

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Product Details of [ 113589-26-7 ]

CAS No. :113589-26-7
Formula : C7H7BrO3S
M.W : 251.10
SMILES Code : O=C(C1=C(O)C(Br)=C(C)S1)OC
MDL No. :MFCD17012774
Boiling Point : No data available

Safety of [ 113589-26-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P305+P351+P338-P332+P313-P337+P313-P362

Application In Synthesis of [ 113589-26-7 ]

* 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 [ 113589-26-7 ]

[ 113589-26-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 5556-22-9 ]
  • [ 113589-26-7 ]
  • 2
  • [ 5556-22-9 ]
  • sodium thiosulfate [ No CAS ]
  • [ 113589-26-7 ]
YieldReaction ConditionsOperation in experiment
With bromine; In (2S)-N-methyl-1-phenylpropan-2-amine hydrate; acetic acid; EXAMPLE 4 Methyl 4-bromo-3-hydroxy-5-methyl-2-thiophenecarboxylate Bromine (4.6 g, 29 mmoles) is added dropwise at room temperature to a stirred solution of <strong>[5556-22-9]methyl 3-hydroxy-5-methyl-2-thiophenecarboxylate</strong> (5.0 g, 29 mmoles) in acetic acid (25 mL). After 16 hours the mixture is stirred into ice water (200 ml), and the precipitate is filtered off, rinsed with water, with 5% aqueous sodium thiosulfate, again with water and dried. Recrystallization from methyl t-butyl ether gave the pure product (4.1 g); mp 96-97 C.
With bromine; In (2S)-N-methyl-1-phenylpropan-2-amine hydrate; acetic acid; EXAMPLE 4 Methyl 4-bromo-3-hydroxy-5-methyl-2-thiophenecarboxylate. Bromine (4.6 g, 29 mmoles) is added dropwise at room temperature to a stirred solution of <strong>[5556-22-9]methyl 3-hydroxy-5-methyl-2-thiophenecarboxylate</strong> (5.0 g, 29 mmoles) in acetic acid (25 mL). After 16 hours the mixture is stirred into ice water (200 mL), and the precipitate is filtered off, rinsed with water, with 5% aqueous sodium thiosulfate, again with water and dried. Recrystallization from methyl t-butyl ether gave the pure product (4.1 g); mp 96-97C.
 

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