Process for preparing solutions of alkali metal salts of...

Organic compounds -- part of the class 532-570 series – Organic compounds – Oxygen containing

Reexamination Certificate

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Reexamination Certificate

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10704808

ABSTRACT:
Alkali metal salt of formula (I): MOYXR1(I), and its solution can be prepared in high yields, particularly high space-time yields, and with high purities by reacting an alcohol of the formula (Ia): HOYXR1(Ia), in a solvent mixture with an alkali metal salt of formula (II): MOR2(II), or by reacting the alcohol (Ia) in a solvent mixture with an alkali metal hydroxide. Part of the liberated alcohol of formula (IIa): HOR2(IIa) or a part of the liberated water is distilled from the solvent mixture, initially, without addition of an entrainer. Subsequently, a remainder of the liberated alcohol of formula (IIa) or the liberated water is distilled from the solvent mixture with the aid of at least one organic solvent as entrainer. In formula (I) and in formula (II), M is Li, Na, K, Rb or Cs. In formula (I) and in formula (Ia): Y is (C1-C8)-alkylene, X is O, S or NR1, and R1is H, (C1-C8)-alkyl, (C2-C8)-alkenyl, (C2-C8)-alkynyl, (C3-C8)-cycloalkyl, (C6-C18)-aryl, (C7-C19)-aralkyl, (C3-C18)-heteroaryl, (C4-C19)-heteroaralkyl, ((C1-C8)-alkyl)1-3-(C3-C8)-cycloalkyl, ((C1-C8)-alkyl)1-3-(C6-C18)-aryl or ((C1-C8)-alkyl)1-3-(C3-C18)-heteoraryl. In formula (II) and in formula (IIa), R2is methyl, ethyl, propyl, isopropyl, sec-butyl, isobutyl or tert-butyl.

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U.S. Appl. No. 10/457,570, filed Jun. 10, 2003, Koehler et al.
U.S. Appl. No. 10/805,257, filed Mar. 22, 2004, Ruwwe et al.
U.S. Appl. No. 10/704,808, filed Nov. 12, 2003, Ruwwe et al.

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