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Chemical Structure| 1095010-50-6 Chemical Structure| 1095010-50-6

Structure of 1095010-50-6

Chemical Structure| 1095010-50-6

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Product Details of [ 1095010-50-6 ]

CAS No. :1095010-50-6
Formula : C6H6BrNS
M.W : 204.09
SMILES Code : BrC1=NC(=CS1)C1CC1
MDL No. :MFCD11656783

Safety of [ 1095010-50-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1095010-50-6 ]

* 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 [ 1095010-50-6 ]

[ 1095010-50-6 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 324579-90-0 ]
  • [ 1095010-50-6 ]
YieldReaction ConditionsOperation in experiment
43% With tert.-butylnitrite; copper(I) bromide; In acetonitrile; at 0 - 20℃; for 0.5h; To a stirred solution of Compound J (5.6 g, 40 mmol) and CuBr (8.5 g, 60 mmol) in CH3CN (100 mL) was added dropwise t-BuONO (6.2 g, 7.2 mL, 60 mmol) at 0 °C. Then the reaction mixture was warmed to room temperature and further stirred for additional 30 mins. After that, the precipitate was filtered and the solvent was removed under reduced pressure. The residue was purified by column chromatography (eluent: 100percent petroleum ether) to afford the desired product K (3.5 g, 43 percent) as a light yellow oil containing small amount of petroleum ether. 1H NMR (400 MHz, CDC13): delta 6.77 (s, 1H), 2.00-1.95 (m, 1H), 0.94-0.85 (m, 4H).
43% With acetonitrile; copper(I) bromide; sodium t-butanolate; at 0 - 20℃; for 0.5h; To a stirred solution of Compound J (5.6 g, 40 mmol) and CuBr (8.5 g, 60 mmol) in CH3CN (100 mL) was added dropwise t-BuONO (6.2 g, 7.2 mL, 60 mmol) at 0° C. Then the reaction mixture was warmed to room temperature and further stirred for additional 30 mins. After that, the precipitate was filtered and the solvent was removed under reduced pressure. The residue was purified by column chromatography (eluent: 100percent petroleum ether) to afford the desired product K (3.5 g, 43percent) as a light yellow oil containing small amount of petroleum ether. 1H NMR (400 MHz, CDCl3): delta 6.77 (s, 1H), 2.00-1.95 (m, 1H), 0.94-0.85 (m, 4H).
 

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