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Chemical Structure| 81168-17-4 Chemical Structure| 81168-17-4

Structure of 81168-17-4

Chemical Structure| 81168-17-4

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Product Details of [ 81168-17-4 ]

CAS No. :81168-17-4
Formula : C14H24O2Si
M.W : 252.42
SMILES Code : OCC1=CC=CC=C1CO[Si](C)(C(C)(C)C)C

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Application In Synthesis of [ 81168-17-4 ]

* 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 [ 81168-17-4 ]

[ 81168-17-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 14437-03-7 ]
  • [ 81168-17-4 ]
  • C23H33NO5SSi [ No CAS ]
YieldReaction ConditionsOperation in experiment
99% With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; toluene; at 0 - 20℃; for 4h; (b) Compound II (3.78 g, 15.0 mmol) and THF (100 mL, tetrahydrofuran) were added to a 250 mL three-necked flask.Compound II is dissolved and cooled to 0 ° C;Methyl toluenesulfonyl carbamate (3.61 g, 15.8 mmol),Triphenylphosphine (4.33g, 16.5mmol)And diethyl azodicarboxylate (DEAD, 7.5 mL, 40 wtpercent toluene solution, 1.65 mmol);Stir at room temperature for 4 hours,TLC showed complete reaction;Pump concentration,Purification by column to obtain 6.89 g of compound III (purity: 99.5percent).
6.89 g With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; toluene; at 0 - 20℃; for 4h; (b)in 250 ml of three compound is added in the bottle II (3.78 g, 15.0 mmol), THF (100 ml, namely tetrahydrofuran), making compound II dissolved and lowering the temperature to 0 °C; adding <strong>[14437-03-7]methyl tosylcarbamate</strong> (3.61 g, 15.8 mmol), triphenylphosphine (4.33 g, 16.5 mmol) and Diethyl dicarboxylate(DEAD, 7.5 ml, 40 wt percent toluene solution, 1.65 mmol); stirring at room temperature 4 hours, TLC shows the reaction is complete; water pump concentrated, column purified 6.89 g compound III (purity 99.5percent).
6.89 g With triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; toluene; at 0 - 20℃; for 4h; (b) Compound II (3.78 g, 15.0 mmol), THF (100 mL, tetrahydrofuran) was added to a 250 mL three-necked flask, and the compound II was dissolved and cooled to 0 ° C;Add <strong>[14437-03-7]methyl tosylcarbamate</strong> (3.61 g, 15.8 mmol), triphenylPhosphine (4.33g, 16.5mmol) and diethyl azodicarboxylate (DEAD, 7.5mL, 40wtpercent toluene solution, 1.65mmol); room temperatureAfter stirring for 4 hours, TLC showed the reaction was complete; the water was concentrated and purified by column to yield 6.89 g of Compound III (purity99.5percent)
 

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