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Chemical Structure| 23095-03-6 Chemical Structure| 23095-03-6

Structure of 23095-03-6

Chemical Structure| 23095-03-6

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Product Details of [ 23095-03-6 ]

CAS No. :23095-03-6
Formula : C7H8BrNO3S
M.W : 266.11
SMILES Code : O=S(C1=CC=C(OC)C(Br)=C1)(N)=O
MDL No. :MFCD02135252

Safety of [ 23095-03-6 ]

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

Application In Synthesis of [ 23095-03-6 ]

* 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 [ 23095-03-6 ]

[ 23095-03-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 23094-96-4 ]
  • [ 23095-03-6 ]
YieldReaction ConditionsOperation in experiment
100% With ammonia; triethylamine; In 1,4-dioxane; dichloromethane; for 2h; 3-Bromo-4-methoxyphenylsulfonyl chloride (2.80 g, 9.8 mmol) was dissolved in dichloromethane (200 mL) and the solution treated with a solution of 0.5 M ammonia in dioxane (100 mL) and triethylamine (5 mL) for 2 hours. The reaction mixture was poured onto a mixture consisting of a 5% citric acid solution and dichloromethane. The organic layer was separated and the aqueous layer was extracted dichloromethane. The extracts were dried and concentrated to give 3-bromo-4-methoxyphenylsulfonamide (2.65 g, 100%).
With ammonia; triethylamine; In 1,4-dioxane; dichloromethane; at 0 - 20℃; for 2h; 14 g of <strong>[23094-96-4]3-bromo-4-methoxybenzenesulfonyl chloride</strong> obtained in Reference Example 11(a) was dissolved in dichloromethane (1000 mL), and then 0.5 M ammonia solution in 1,4-dioxane (518 mL) and triethylamine (26 mL) were added thereto at 0 C., followed by stirring at room temperature for 2 hours. The formation of the product was confirmed by TLC, and 5% aqueous solution of citric acid was added to stop the reaction, followed by extraction using ethyl acetate. Thereafter, the organic phase was dried over anhydrous magnesium sulfate, followed by filtration, and thus obtaining 11.4 g of the title compound as a crude product by vacuum concentration of the filtrate.MS (ESI) m/z: 266 (M+H)+
 

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