Method for oxidation of xylene derivatives

Organic compounds -- part of the class 532-570 series – Organic compounds – Carboxylic acids and salts thereof

Reexamination Certificate

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C562S412000, C562S888000, C562S897000

Reexamination Certificate

active

06465685

ABSTRACT:

BACKGROUND OF THE INVENTION
This invention relates to a method for oxidizing xylene derivatives. More particularly, the invention relates to a method for oxidizing a substrate comprising at least one halo-ortho-xylene in the presence of at least one metal catalyst, at least one solvent, and at least one promoter to provide a product comprising halo-phthalic acid or halo-phthalic anhydride. In one key embodiment the invention relates to a method for producing a product comprising 4-chlorophthalic acid or 4-chlorophthalic anhydride.
Methods for oxidizing ortho-xylene are known. For example, U.S. Pat. No. 3,402,184 describes oxidation of ortho-xylene in acetic acid solvent in the presence of a bromine promoter. U.S. Pat. Nos. 5,958,821, 5,981,420, and 6,020,522 describe oxidation of ortho-xylene in acetic acid solvent in the presence of a hydroxyimide promoter. Methods for preparing 4-chlorophthalic anhydride are also known. However, these methods typically involve aromatization of a Diels-Alder adduct of chloroprene and a maleic anhydride as in U.S. Pat. No. 5,322,954, or chlorination of phthalic acid as in Japanese patent applications 07258152 and 02129143. The latter chlorination process may produce polychlorinated biphenyls (PCBs). There is a need for a method for producing 4-chlorophthalic anhydride which does not involve handling toxic chloroprene or chlorine gas, and which does not produce PCBs.
SUMMARY OF THE INVENTION
In one embodiment the invention is a method for oxidizing a substrate comprising at least one halo-ortho-xylene which comprises combining the substrate in a solvent with at least one metal catalyst and heating in the presence of an oxygen source to produce a product mixture, wherein an effective amount of at least one promoter is added to the reaction mixture after the reaction has proceeded to an intermediate stage of conversion to product mixture.
In another embodiment the invention is a method for oxidizing a substrate comprising 4-chloro-ortho-xylene which comprises combining chloro-ortho-xylene in acetic acid solvent with at least one metal catalyst which is a metal compound comprising cobalt, and heating in the presence of an oxygen source to produce a product mixture comprising 4-chlorophthalic acid or 4-chlorophthalic anhydride, wherein an effective amount of at least one promoter is added to the reaction mixture after the reaction has proceeded to an intermediate stage of conversion to product mixture.
In still another embodiment the invention is a method for producing a product mixture comprising 4-chlorophthalic acid or 4-chlorophthalic anhydride which comprises oxidizing a substrate comprising 4-chloro-ortho-xylene, optionally in the presence of chlorotoluic acid, which comprises the steps of
(i) combining substrate in acetic acid solvent with at least one metal catalyst comprising cobalt, and optionally manganese, and heating in the presence of an oxygen source to a temperature in a range of between about 100° C. and about 230° C. at pressure in a range of between about 1300 and about 8300 kilopascals, wherein the molar ratio of substrate to the at least one metal catalyst is in a range of about 80-250:1;
(ii) adding, after the conversion to product mixture has reached about 35-65%, an effective amount of at least one promoter selected from the group consisting of N-hydroxyphthalimide, 4-chloro-N-hydroxyphthalimide, 3-chloro-N-hydroxyphthalimide, dichloro-N-hydroxyphthalimide, N-hydroxymaleimide, N-hydroxysuccinimide, 2-carboxyphenylhydroxamic acid, 4-chloro-2-methylbenzaldehyde, tetraethylammonium bromide, tetrabutylammonium bromide, and sodium bromide;
(iii) heating the reaction mixture under pressure of oxygen source to increase conversion to product mixture; and
(iv) isolating product comprising 4-chlorophthalic acid or 4-chlorophthalic anhydride.


REFERENCES:
patent: 3402184 (1968-09-01), Bethoux et al.
patent: 4215053 (1980-07-01), Palmer et al.
patent: 4299977 (1981-11-01), Kuhlmann et al.
patent: 4322549 (1982-03-01), Kuhlmann et al.
patent: 4387243 (1983-06-01), Naim et al.
patent: 4436922 (1984-03-01), Kita et al.
patent: 4992580 (1991-02-01), Partenheimer
patent: 5112992 (1992-05-01), Belmonte et al.
patent: 5225573 (1993-07-01), Shorr et al.
patent: 5229482 (1993-07-01), Brunelle
patent: 5322954 (1994-06-01), Seper et al.
patent: 5359133 (1994-10-01), Nazimok et al.
patent: 5830974 (1998-11-01), Schmidhauser et al.
patent: 5958821 (1999-09-01), Ishii et al.
patent: 5981420 (1999-11-01), Nakano et al.
patent: 6020522 (2000-02-01), Ishii et al.
patent: 22 36 875 (1974-03-01), None
patent: 0 539 878 (1996-01-01), None
patent: 0 879 812 (1998-11-01), None
patent: 02129143 (1990-05-01), None
patent: 07258152 (1995-10-01), None
patent: 722909 (1980-03-01), None
patent: 1 719 401 (1992-03-01), None
patent: WO98/17608 (1998-04-01), None
patent: WO98/37967 (1998-09-01), None
Liquid-Phase Catalytic Oxidation of 4-Bromo-o-Xylene, 6001 Chemical Abstracts, Columbus, Ohio, U.S. vol. 90, 38640, No. 5, G. Uzulneice et al., Latv. PSR Zinat. Akad, Vestis, Kim. Ser. 1978, vol. 5, pp. 617-620.
Preparation of Monochlorophthalic Acids By the Liquid-Phase Catalytic Oxidation of Chloro-o-Xylenes, , 6001 1984, vol. 50(6), pp. 644-647.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Method for oxidation of xylene derivatives does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Method for oxidation of xylene derivatives, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Method for oxidation of xylene derivatives will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2968091

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.