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ChemicalBook CAS DataBase List BENZYL PHENYL CARBONATE 97

BENZYL PHENYL CARBONATE 97 synthesis

4synthesis methods
-

Yield:28170-07-2 78%

Reaction Conditions:

with ethyl(8-diisopropylamino-3,6-dioxaoctyl)dimethylammonium bis{(trifluoromethyl)sulfonyl}azanide at 25; under 7500.75 Torr; for 72 h;Autoclave;Green chemistry;

Steps:

Experimental
General procedure: All the reactions were carried out in a 16 mL stainless-steelautoclave with stirring at 600 rpm and equipped with an automatic stirrer and temperature control system. In a typicalreaction procedure, IL (0.60 mmol, 1.2 equiv.), benzyl bromide(0.5 mmol, 85.5 mg, 1.0 equiv.), and alcohols (1.0 mmol, 2.0equiv.) were added into the autoclave successively. CO2 (1.0MPa) was charged into the reactor at room temperature. The autoclave was stirred at 25°C for an appropriate time. Afterreaction, the excess of CO2 was vented. Ethyl ether (2 mL) was added to the mixture, and the crude product was extracted intothe ether layer. The pure product was obtained after evaporation of solvent and excess starting materials.

References:

Goodrich, Peter;Gunaratne, H. Q. Nimal;Jin, Lili;Lei, Yuntao;Seddon, Kenneth R. [Australian Journal of Chemistry,2018,vol. 71,# 2-3,p. 181 - 185]

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