Hydrogenation of fluorinated esters
AssigneeAllied Chemical Corporation
InventorsHenry R. Nychka, Richard E. Eibeck, Martin A. Robinson, Edward S. Jones
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AssigneeAllied Chemical Corporation
InventorsHenry R. Nychka, Richard E. Eibeck, Martin A. Robinson, Edward S. Jones
Estimating the term…
Fluorinated esters of the formula C.sub.n H.sub.x F.sub.2n+1-x CO.sub.2 CH.sub.2 C.sub.m H.sub.y F.sub.2m+1-y such as CF.sub.3 CO.sub.2 CH.sub.2 CF.sub.3 are hydrogenated to fluorinated alcohols such as CF.sub.3 CH.sub.2 OH using a catalyst having between 50 and 100 percent, and preferably 75-95 percent CuO by weight. In the above formula n= 1 to 13, m= 1 to 13, x= 0 to 3 and y= 0 to 3. In the most preferred esters, n= m and x= y= 0. The catalyst may also contain 0-50 percent and preferably 5-25 percent by weight of a filler or binder such as a silicate salt. The reaction produces greater yields of alcohol and longer catalyst life than with chromite catalysts, and may proceed at substantially atmospheric pressures.
A method for the preparation of fluorinated alcohols of the formula C.sub.n H.sub.x F.sub.2n+1-x CH.sub.2 OH, wherein n=1 to 13 and x=0 to 3 but not more than n, comprising passing at between about 200.degree. C and about 325.degree. C a vaporous mixture of hydrogen and a fluorinated ester of the formula C.sub.n H.sub.x F.sub.2n+1-x CO.sub.2 CH.sub.2 -- C.sub.m H.sub.y F.sub.2m+1-y, wherein n and x are as described above and m=1 to 13 and y=0 to 3 but not more than m, over a catalyst consisting essentially of about 50 to 100 percent by weight CuO and 0 to about 50 percent by weight of an inert base or binder, said catalyst being essentially free of chromite, and recovering the fluorinated alcohol.
Dependencies are inferred from the claim text.