Phosphine oxide, (diethoxymethyl)diphenyl-
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20570-20-1CCOC(OCC)P(=O)(c1ccccc1)c1ccccc1LKSRYMVZGUQOFC-UHFFFAOYSA-N20570-20-1DTXSID40174577CHEMBL1430560安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。
解説酸素原子を陰性成分としてもつ化合物.たとえば,二酸化炭素CO2,酸化鉄(III)Fe2O3など.
使用(Diethoxymethyl)diphenylphosphine Oxide is a readily accessible Horner-Wittig reagent for the conversion of aldehydes and ketones into homologous O,O-ketene acetals.[1]
製造方法(Diethoxymethyl)diphenylphosphine Oxide (1) can be conveniently prepared by reaction of Chlorodiphenylphosphine with Triethyl Orthoformate. [2] Adduct (2) is formed in a fast, exothermic, step. Upon heating, an Arbuzov reaction occurs to give the phosphine oxide (eq 1). Other O,O-acetals of formyldiphenylphosphine oxide can be prepared equally well. The usual procedure is for chlorodiphenylphosphine (88.2 g, 0.4 mol) to be added dropwise to triethyl orthoformate (59.3 g, 0.4 mol) over a period of 45 min. Subsequent heating of the reaction mixture (2 h, 110 °C) leads to formation of 24 g (93% of theory) of ethyl chloride. Upon cooling, a practically quantitative yield of (1) is obtained, mp 74-77 °C. Addition of some solvent, when (1) starts precipitating, avoids the formation of a solid cake that is hard to remove from the reaction flask. Crystallization from benzene/petroleum ether (80-110) affords the pure phosphine oxide.
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