Method for producing dithiine tetracarboximides

Patent metadata

Field	Value
Publication number	US-9365586-B2
Application number	US-201314385648-A
Country	US
Kind code	B2
Filing date	Mar 18, 2013
Priority date	Mar 23, 2012
Publication date	Jun 14, 2016
Grant date	Jun 14, 2016

Abstract

The present invention relates to a process for preparing dithiinetetracarboximides by reaction of succinic monoamides with thionyl chloride, with continuous performance of at least one of the process steps.

First claim

The invention claimed is:

1. A process for preparing a dithiinetetracarboximide of formula (I)

in which
R 1 and R 2 are the same or different and are each
(i) hydrogen,
(ii) optionally mono- or poly-halogen-, —OR 3 —, —COR 4 -substituted C 1 -C 8 -alkyl,
(iii) optionally mono- or poly-halogen-, —C 1 -C 4 -alkyl- or —C 1 -C 4 -haloalkyl-substituted C 3 -C 7 -cycloalkyl,
(iv) optionally mono- or poly-halogen-, —C 1 -C 4 -alkyl-, —C 1 -C 4 -haloalkyl-, —COR 4 —or -sulphonylamino-substituted aryl, or
(v) aryl-(C 1 -C 4 -alkyl),
R 3 is hydrogen, C 1 -C 4 -alkyl, C 1 -C 4 -alkylcarbonyl, or (vi) optionally mono- or poly-halogen-, —C 1 -C 4 -alkyl- or —C 1 -C 4 -haloalkyl-substituted aryl,
R 4 is hydroxyl, C 1 -C 4 -alkyl, or C 1 -C 4 -alkoxy,
comprising:
(1) reacting a succinic monoamide of formula (VI)

in which R is R 1 or R 2
with thionyl chloride to give a reaction mixture,
(2) heating the reaction mixture formed in a second stage (2), and then
(3) converting the reaction mixture to one or more dithiinetetracarboximides in a third stage (3),
with continuous performance of at least one of (1), (2) and/or (3).

2. The process according to claim 1 , wherein the total amount of thionyl chloride (z) is from 2.5 to 20 mol per mole of succinic monoamide of the formula (VI), where z is defined by the relationship
z=x+y

and
z is a total amount of thionyl chloride (mol of thionyl chloride per mole of succinamide of formula (VI)) in (1) and (2),
x is the amount of thionyl chloride in (1) and
y is the amount of thionyl chloride additionally used in (2).

3. The process according to claim 2 , wherein the value z is from 2.5 to 14 mol per mole of succinic monoamide of the formula (VI).

4. The process according to claim 2 , wherein the value z is from 2.5 to 9 mol per mole of succinic monoamide of the formula (VI).

5. The process according to claim 2 , wherein the amount of thionyl chloride x in (1) is from 1 to 20 mol per mole of succinic monoamide of the formula (VI).

6. The process according to claim 1 , wherein abatement of evolution of gas in (2) is followed by conversion of the reaction mixture to one or more dithiinetetracarboximides in (3).

7. The process according to claim 6 , wherein a resulting intermediate is dissolved in a diluent, admixed with water to form a mixture and converted to one or more dithiinetetracarboximides of the formula (I) by heating in said mixture.

8. The process according to claim 1 , wherein (1) is performed continuously.

9. The process according to claim 1 , wherein (2) is performed continuously.

10. The process according to claim 1 , wherein an organic solvent at least partly miscible with water is used in (3).

11. The process according to claim 1 , wherein at least one solvent used in (3) comprises water, dimethyl sulphoxide, sulpholane, alcohols optionally comprising methanol, ethanol, propanol, isopropanol, 1-butanol, 2-butanol, isobutanol, tert-butanol, 1-pentanol, cyclopentanol, cyclohexanol, ethylene glycol, ethylene glycol monomethyl ether, hydrocarbons optionally comprising hexane, heptane, cyclohexane, methylcyclohexane, toluene, xylenes, mesitylene, chlorobenzene, dichlorobenzene, nitrobenzene, esters optionally comprising methyl acetate, ethyl acetate, amides such as formamide, N,N-dimethylformamide; N,N-dimethylacetamide, N-methylpyrrolidone, ethers optionally comprising methyl tert-butyl ether, tetrahydrofuran, 1,4-dioxane, nitriles optionally comprising acetonitrile, propionitrile, butyronitrile, benzonitrile, ketones optionally comprising acetone, methyl ethyl ketone, methyl isobutyl ketone, pinacolone, carboxylic acids optionally comprising formic acid, acetic acid, propionic acid, or a mixture thereof.

12. The process according to claim 1 , wherein (3) is performed at a reaction temperature from 40° C. to 120° C.

13. The process according to claim 1 , wherein (3) is performed continuously.

14. The process according to claim 2 , wherein additional thionyl chloride is used in (2).

Assignees

• Bayer Cropscience Ag
• Bayer Ip Gmbh

Inventors

• Himmler Thomas
• Geller Thomas
• Rodefeld Lars
• Ford Mark James
• Hoemberger Guenter
• Heinz Dieter

Classifications

• C07D495/14 Primary

  Ortho-condensed systems · CPC title