tert-butyl 2-((1R,3S)-3-hydroxycyclohexylmethoxy)-2-methylpent-4-enoate                                                                                                                                                              在
                                                                                                                                         
钯                                                                                                                                                                                                                               氢气   、                                                                                                  
tert-butyl 2-((1R,3S)-3-hydroxycyclohexylmethoxy)-2-methylpentanoate                                                                                                                                  作用下,
                                                                                                                以
                                                                                         
乙酸乙酯                                                                                  为溶剂,
                                                                                                                                                            25.0 ℃
                                                                                                                            、40.0 MPa
                                                                                条件下,
                                                                                                                反应 16.0h,
                                                                                                                以resulting in 2.3 g of tert-butyl 2-((1R,3S)-3-hydroxycyclohexylmethoxy)-2-methylpentanoate as a mixture of two iastereomers as pale yellow oil的产率得到tert-butyl 2-((1R,3S)-3-hydroxycyclohexylmethoxy)-2-methylpentanoate