“…Alternatively, transesterification using ethyl acetate (EtOAc) has attracted much attention in recent years, since the reaction can be environmentally friendly, ideally producing only ethanol as a byproduct. Therefore, many useful transesterification reactions of alcohols with ethyl acetate using LiAl(O n C 8 H 17 ) alumina, metallic sulfates, PPh 3 /CBr 4 , Ce(OTf) 4 , distannoxane, In/I 2 , K 5 CoW 12 O 40 ⋅3H 2 O, N ‐hetrocyclic carbene, silphos, H 3 PW 12 O 40 , Zn 4 (OCOCF 3 ) 6 O, amberlyst‐15, silica‐bonded N ‐propyl sulfamic acid, lanthanum(III) catalyst, NaO t Bu, KO t Bu, I 2 , and enzymes have been reported. However, since most of these reactions require heating or strong bases (Scheme (a)), the development of a reaction that proceeds under mild conditions (Scheme (b)) is desired.…”