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