(1S)-1-苯乙烷-1,2-二醇

反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: Regarding Example 31, except that the use amount of RuCl[(S)-xylbinap][(S)-daipen] was changed (3.0 mg, 0.0025 mol, 1/1,000 molar fold of 2-hydroxyacetophenone) and 2-propanol (2.5 mL) was used instead of methanol, the same procedure as Example 31 was carried out. As a result of analysis of the reaction solution by using gas chromatography (HP-1), the conversion rate was found to be 99% or more. The optical purity was measured by high performance liquid chromatography (CHIRALPAK AS-H, eluent; hexane:2-propanol=92:8), and it was found to be 90% ee. As a result of analysis of the reaction solution

反应条件: temp:30.01; pressure:0.00; stir:; See reaction.notes.procedure_details.

实验步骤: To a 100 mL autoclave with a stirrer, 2-hydroxyacetophenone (340 mg, 2.5 mmol) and RuCl[(S)-xylbinap][(S)-daipen] obtained from the Example 1 above (1.5 mg, 0.00125 mol, 1/2,000 molar fold of 2-hydroxyacetophenone) were added. After purging with nitrogen, methanol (1.25 mL) and 1,8-diazabicyclo[5.4.0]undeca-7-ene (1.9 mg, 0.0125 mmol) were added. Subsequently, purging with hydrogen, the mixture was stirred at 30° C. for 5 hours under hydrogen pressure of 1 MPa. As a result of analysis of the reaction solution by using gas chromatography (HP-1), the conversion rate was found to be 99% or more. The optical purity was measured by high performance liquid chromatography (CHIRALPAK AS-H, eluent; hexane:2-propanol=92:8), and it was found to be 94% ee. were added were added Subsequently, purging with hydrogen As a result of analysis of the reaction solution