Claims
- 1. A process for the preparation of 1,1'-oxy-bis(3-trifluoromethyl-4-nitrobenzene) which comprises reacting in a non-polar solvent or in the absence of a solvent a compound of the formula ##STR4## where X is F, Cl, Br, or I with up to a stoichiometric amount of an inorganic base selected from the group consisting of alkali metal hydroxides, alkali metal carbonates, and alkali metal bicarbonates, in the presence of a small amount of water, at least about 0.1 mole % of a benzoate catalyst and a phase transfer catalyst when a non-polar solvent is present.
- 2. A process according to claim 1 conducted in a non-polar solvent.
- 3. A process according to claim 2 wherein the inorganic base is sodium carbonate or potassium carbonate.
- 4. A processing according to claim 2 wherein the inorganic base is sodium hydroxide or potassium hydroxide.
- 5. A process according to claim 1 conducted in the absence of a solvent.
- 6. A process according to claim 5 wherein the inorganic base is sodium carbonate or potassium carbonate.
- 7. A process according to claim 5 wherein the inorganic base is sodium hydroxide or potassium hydroxide.
- 8. A process according to claim 1 wherein the reaction temperature is between about 110 and 220.degree. C.
- 9. A process according to claim 1 wherein said benzoate catalyst is a benzoate ester of 4-nitro-3-trifluoromethylphenol.
- 10. A method of preparing 1,1'-oxy-bis(3-trifluoromethyl-4-nitrobenzene) comprising
- (A) preparing a reaction mixture which comprises
- (1) a compound having the formula ##STR5## where X is F or Cl; (2) up to a stoichiometric amount of sodium carbonate;
- (3) at least about 0.1 mole % of benzoate catalyst selected from the group consisting of benzoic acid, chlorobenzoic acids, bromobenzoic acids, fluorobenzoic acids, dichlorobenzoic acids, dibromobenzoic acids, difluorobenzoic acids, tribromobenzoic acids, trichlorobenzoic acids, trifluorobenzoic acids, trifluoromethylbenzoic acids, nitrobenzoic acids, dinitrobenzoic acids, C.sub.1 to C.sub.12 alkylbenzoic acids, C.sub.1 to C.sub.12 alkoxybenzoic acids, C.sub.2 to C.sub.12 acyloxybenzoic acids, and salts thereof;
- (4) a minimal amount of water;
- (5) an optional non-polar solvent; and
- (6) a phase transfer catalyst if said non-polar solvent is present; and
- (B) heating said reaction mixture between about 110 and 220.degree. C.
- 11. A process according to claim 10 wherein X is Cl.
BACKGROUND OF THE INVENTION
This application is a continuation-in-part of U.S. application Ser. No. 07/669,707, filed Mar. 15, 1991, and now abandoned.
US Referenced Citations (2)
Number |
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Date |
Kind |
4558164 |
Jones et al. |
Dec 1985 |
|
4700011 |
Pillsbury |
Oct 1987 |
|
Foreign Referenced Citations (1)
Number |
Date |
Country |
24125 |
Feb 1980 |
JPX |
Non-Patent Literature Citations (2)
Entry |
Mari et al., Gov. Industrial Research Institute, No. 3, 675-677, "Synthesis of Diisobyanates of Trifluoromethyl Substituted Biphenyls and Diphenyls", 1972. |
Jacobs, J. Org. Chem., vol. 36, No. 1, pp. 242-243, 1971, "Synthesis of Nitrotrifluoromethylphenols and Related Compounds . . .". |
Continuation in Parts (1)
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Number |
Date |
Country |
Parent |
669707 |
Mar 1991 |
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