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Synthesis of ruthenium-hydride complexes and preparation procedures of chiral alcohols and ketones

机译:氢化钌配合物的合成及手性醇和酮的制备方法

摘要

trans-RuH(&eegr;1-BH4)[(S)-xylbinap][(S,S)-dpen] (0.00125 mmol), acetophenone (5.0 mmol), and 2-propanol (2.5 mL) were placed in an autoclave, and the resulting solution was repeatedly subject 5 times to a procedure of performing pressure reduction and argon introduction while stirring the solution for deaeration. A hydrogen tank was then connected to the autoclave, and after replacing the air inside an introduction tube with hydrogen, the pressure inside the autoclave was adjusted to 5 atmospheres and then hydrogen was released until the pressure dropped to 1 atmosphere. After repeating this procedure 10 times, the hydrogen pressure was adjusted to 8 atmospheres and stirring at 25° C. was performed for 12 hours. By concentrating the solution obtained by depressurization and subjecting the crude product to simple distillation, (R)-1-phenylethanol (yield: 95%) in the form of a colorless oily substance was obtained at an ee of 99%.
机译:反式RuH(&eegr; 1 -BH 4 )[(S)-xylbinap][(S,S)-dpen]将(0.00125mmol),苯乙酮(5.0mmol)和2-丙醇(2.5mL)放入高压釜中,将所得溶液重复进行5次减压和引入氩气的步骤,同时搅拌该溶液以进行脱气。 。然后将氢气罐连接至高压釜,并且在用氢气代替引入管内的空气之后,将高压釜内的压力调节至5个大气压,然后释放氢气直至压力降至1个大气压。重复该步骤10次之后,将氢气压力调节至8个大气压,并在25℃下搅拌。进行12小时。通过浓缩通过减压获得的溶液并将粗产物进行简单蒸馏,以99%的ee得到无色油状物形式的(R)-1-苯基乙醇(收率:95%)。

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