骨化三醇   、                                                                                      
(12R)-acetoxyoleic acid                                                                                                                                                              在
                                                                                                                                                                                 
N,N'-二环己基碳二亚胺   、                                                                                                  
4-二甲氨基吡啶                                                                                                                                  作用下,
                                                                                                                以
                                                                                         
四氢呋喃   、                                                                                         
二氯甲烷                                                                                  为溶剂,
                                                                                                                                                    反应 14.25h,
                                                                                                                生成                                                 (1R,3S,Z)-3-hydroxy-5-(2-((1R,3aS,7aR,E)-1-((R)-6-hydroxy-6-methylheptan-2-yl)-7a-methyloctahydro-4H-inden-4-ylidene)ethylidene)-4-methylenecyclohexyl (R,Z)-12-acetoxyoctadec-9-enoate   、                                                                                             (1S,5R,Z)-5-hydroxy-3-(2-((1R,3aS,7aR,E)-1-((R)-6-hydroxy-6-methylheptan-2-yl)-7a-methyloctahydro-4H-inden-4-ylidene)ethylidene)-2-methylenecyclohexyl (R,Z)-12-acetoxyoctadec-9-enoate