Racemization process for optically active carboxylic acids or salts or esters thereof
AssigneeAlbemarle Corporation
InventorsRobert E. Young, Hao V. Phan, Thanikavelu Manimaran, Ronald C. Zumstein
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AssigneeAlbemarle Corporation
InventorsRobert E. Young, Hao V. Phan, Thanikavelu Manimaran, Ronald C. Zumstein
Estimating the term…
Optically active carboxylic acids, salts or esters, such as the profen-type compounds, are racemized in the presence by nitrogenous bases such as methylbenzylamine by heating an aqueous solution of such optically active compounds in the presence of a suitable excess of an alkali metal hydroxide relative to the amount optically active carboxylic compound present in the solution. The process not only enables conversion of inactive or undesirable enantiomers of compounds such as naproxen or ibuprofen into a usable, desirable enantiomers in an efficient and economical manner, but avoids conversion of the nitrogenous base into amide. Thus the deleterious consequences of amide formation are avoided.
A method for racemizing in the presence of one or more organic nitrogenous bases, one of the enantiomers, or an enantiometrically enriched mixture, of an optically active carboxylic compound of the formula:
A method for racemizing in the presence of one or more organic nitrogenous bases, one of the enantiomers, or an enantiometrically enriched mixture, of an optically active carboxylic compound of the formula:
A method for racemizing in the presence of one or more organic nitrogenous bases, 2-(6-methoxy-2-naphthyl)propionic acid and/or salt(s) thereof in which less than 50% thereof is the (S)-enantiomeric form thereof, said method comprising:
Dependencies are inferred from the claim text.