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Chemical Structure| 90531-98-9 Chemical Structure| 90531-98-9

Structure of 90531-98-9

Chemical Structure| 90531-98-9

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Product Details of [ 90531-98-9 ]

CAS No. :90531-98-9
Formula : C8H9BrO3S
M.W : 265.12
SMILES Code : O=S(C1=CC=C(Br)C(OC)=C1)(C)=O

Safety of [ 90531-98-9 ]

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

Application In Synthesis of [ 90531-98-9 ]

* 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 [ 90531-98-9 ]

[ 90531-98-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 41608-73-5 ]
  • [ 90531-98-9 ]
YieldReaction ConditionsOperation in experiment
41% With tert.-butylnitrite; copper(ll) bromide; In acetonitrile; at 80.0℃; for 1.0h; Compound 34-e (1.0 g, 4.98 mmol) was dissolved in acetonitrile (10 mL), copper(II) bromide (1.9 g, 7.50 mmol)was added and tert-butyl nitrite (0.73 mL) was added slowly thereto. The reaction mixture was stirred at 80°C for 1 hour.The reaction mixture was cooled to room temperature, diluted with water (50 mL) and extracted with ethyl acetate (100mL). The organic phase was washed successively with water (50 mL 3 3) and brine (50 mL), dried over anhydroussodium sulfate, filtered, and the filtrate was concentrated under reduced pressure. The residue was purified by silica gelcolumn chromatography (petroleum ether: ethyl acetate = 1:1) to delivera pale yellow solid 34-d (540 mg, yield: 41percent).LC-MS (ESI): m/z = 202 [M+H]+.
540 mg With tert.-butylnitrite; copper(I) bromide; In acetonitrile; at 80.0℃; for 1.0h; Compound 4-c (1 g, 4.98 mmol) was dissolved in acetonitrile (10 mL) and copper bromide (1.9 g, 7.50 mmol) was added, followed by slowly adding tert-butyl nitrite (0.73 mL). The mixture was heated to 80° C. and reacted for 1 hour, cooled to room temperature and then concentrated under reduced pressure. The residue was diluted with ethyl acetate (100 mL) and water (50 mL) and filtered through celite. The combined organic phase was dried over anhydrous sodium sulfate, filtered and the filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (petroleum ether: ethyl acetate=1:1) to give 4-b as a pale yellow solid (540 mg, yield 41percent). LC-MS (ESI): m/z=265[M+H]+.
 

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