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Chemical Structure| 56999-16-7 Chemical Structure| 56999-16-7

Structure of 56999-16-7

Chemical Structure| 56999-16-7

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Product Details of [ 56999-16-7 ]

CAS No. :56999-16-7
Formula : C12H26O5
M.W : 250.33
SMILES Code : CCOC(OCC)COCC(OCC)OCC
MDL No. :MFCD09865709

Safety of [ 56999-16-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302
Precautionary Statements:P280-P305+P351+P338

Application In Synthesis of [ 56999-16-7 ]

* 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 [ 56999-16-7 ]

[ 56999-16-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2032-35-1 ]
  • [ 621-63-6 ]
  • [ 56999-16-7 ]
YieldReaction ConditionsOperation in experiment
42% To a suspension of sodium hydride (3.0 g, 60percent dispersion in mineral oil, 125 [MMOL)] in xylenes under nitrogen was added 2, 2-diethoxy-ethanol (15.3 g, 114 [MMOL)] dropwise via canula. The reaction was heated to reflux for two hours, cooled to ambient temperature followed by addition of 2-bromo-1,1-diethoxy-ethane (25.6 mL, 170 [MMOL)] dropwise. The reaction was then heated at reflux overnight. The xylenes were distilled off under atmospheric pressure. The title compound was distilled off under vacuum (6 mm Hg) at [120°C] (12.0 grams, 42 percent yield)
33% To a suspension of NaH (60percent dispersion in mineral oil, 3.8 g, 95.0 mmol) in xylene (100 mL) was added 2,2-diethoxyethanol (1 1.6 g, 86.4 mmol) under N2. The mixture heated at 1 10 °C for 2 hours, then cooled to room temperature and 2-bromo-1 ,1 -diethoxyethane (25.6 g, 130.0 mmol) added. The reaction was heated at 1 10 °C overnight, then cooled to room temperature and the organic layer washed with water, dried (Na2S04), filtered and concentrated. The residue obtained was purified by distillation to give the title compound (7 g, 33percent) as colorless oil.
With potassium iodide; In tetrahydrofuran; diethyl ether; water; mineral oil; Stage I Hydroxyacetaldehyde diethylacetal (3.75 g) was added to sodium hydride (0.8 g, 80percent in mineral oil) in tetrahydrofuran (100 ml) under an atmosphere of nitrogen. The mixture was stirred and bromoacetaldehyde diethyl acetal (5.0 g) and potassium iodide (0.1 g) were added. The mixture was heated to reflux for 16 hours, water added and evaporated under reduced pressure. The residue was dissolved in diethyl ether, the organic phase washed with water, dried (MgSO4) and evaporated under reduced pressure to give bis(2,2-diethoxyethyl)ether, 3.43 g, as a yellow oil. 1 H NMR (CDCl3): delta 1.20(12H,t); 3.60(8H,d); 3.70(4H,q); 4.60(2H,t)ppm.
 

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