Chemical research careers are more diverse than they might first appear, Application of 1273-86-5, as there are many different reasons to conduct research and many possible environments. In a article, mentioned the application of 1273-86-5, Name is Ferrocenemethanol, molecular formula is C11H3FeO
alpha-Ferrocenylalkyl carbonates were demonstrated to be the species for ferrocenylalkylation reactions. The alpha-ferrocenylalkyl carbonates FcCH(R)OCOOEt (1a-c, Fc = ferrocenyl) were easily generated in situ by a reaction of the alpha-ferrocenyl substituted alcohols FcCH(R)OH (5a-c) with equimolar amounts of n-BuLi followed by EtOCOCl in THF or Et2O at 20 C. Due to the low thermal stability, carbonates 1a-c readily undergo a heterolytical decay furnishing the alpha-ferrocenyl carbocations FcCH(R)+ (2a-c) and carbonate anion R’OC(O)O? (3). The last one reversibly loses a molecule of CO2 giving rise anion EtO? that is capable of deprotonating a pre-nucleophile NuH (MeCOCH2COMe, dimethyl malonate, etc.) giving rise the corresponding nucleophile Nu?. The interaction between 2a-c and Nu? produces the alpha-ferrocenylalkylation products FcCH(R)Nu (4a-c) in moderate to high yields. The sequence above is a novel alpha-ferrocenylalkylation procedure easily proceeding under mild and neutral conditions. Due to these features, it may be useful for alpha-ferrocenylalkylations of either thermally labile compounds or the substrates susceptible to acidic conditions. The stability of carbonates 1a-c was found to decrease as the stability of the corresponding carbocations 2a-c increases. With 2-mercapto-1-methylimidazole, the alpha-ferrocenylalkylations proceed as the N-alkylation processes.
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Reference：
Iron Catalysis in Organic Synthesis | Chemical Reviews,
Iron Catalysis in Organic Synthesis: A Critical Assessment of What It Takes To Make This Base Metal a Multitasking Champion