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Chemical Structure| 5853-76-9 Chemical Structure| 5853-76-9

Structure of 5853-76-9

Chemical Structure| 5853-76-9

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Product Details of [ 5853-76-9 ]

CAS No. :5853-76-9
Formula : C6H13BrO
M.W : 181.07
SMILES Code : CC(C)(OCCBr)C
MDL No. :MFCD11196822

Safety of [ 5853-76-9 ]

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

Application In Synthesis of [ 5853-76-9 ]

* 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 [ 5853-76-9 ]

[ 5853-76-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 5853-76-9 ]
  • [ 16001-93-7 ]
  • [ 1428320-10-8 ]
YieldReaction ConditionsOperation in experiment
2a: 1,1-bis(2-t-butoxyethyl)-<strong>[16001-93-7]1,1-bis(dimethylphosphonato)methane</strong> To an ice cooled solution of 1,1-bis(dimethyl)phosphonato)methane (50 g, 215 mmol) in dry THF (500 ml) under nitrogen is added sodium hydride (18.9 g, 60% in mineral oil, 474 mmol) in three portions, over 30 minutes. The mixture is stirred for 3 hours and then 1-bromo-2-t-butoxyethane (90.5 g, 500 mmol) is added in 5 ml portions. The ice bath is removed after three hours and stirring continued at room temperature for overnight. The reaction mixture is cooled with an ice bath again and quenched by the addition of 50 ml saturated aqueous ammonium chloride. The volatiles are removed in vacuo and the organics are dissolved in dichlormethane (300 ml). Silica (100 g) is stirred in and the slurry is filtered and the filter cake is washed with 3 x 200 ml dichloromethane. The product is obtained after removal of the solvents.
To an ice cooled solution of 1 ,1 -bis(dimethyl)phosphonato)nnethane (50 g, 215 mmol) in dry THF (500 ml) under nitrogen is added sodium hydride (18.9 g, 60% in mineral oil, 474 mmol) in three portions, over 30 minutes. The mixture is stirred for 3 hours and then 1 -bromo-2-f-butoxyethane (90.5 g, 500 mmol) is added in 5 ml portions. The ice bath is removed after three hours and stirring continued at room temperature for overnight. The reaction mixture is cooled with an ice bath again and quenched by the addition of 50 ml saturated aqueous ammonium chloride. The volatiles are removed in vacuo and the organics are dissolved in dichlormethane (300 ml). Silica (100 g) is stirred in and the slurry is filtered and the filter cake is washed with 3 x 200 ml dichlo- romethane. The product is obtained after removal of the solvents.
 

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