IP Library Granted Patent US 8,334,417
Granted Patent B2
US 8,334,417 · App. 12/720,247 · Granted Dec 18, 2012

Process for preparing chloro- and bromoaromatics

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Quick Facts
Patent No.
US 8,334,417
App. No.
12/720,247
Granted
Dec 18, 2012
Kind
B2
Abstract

The present invention relates to a novel process for preparing chloro- or bromoaromatics of the formula (II) by diazotizing the formula (I) by means of sodium nitrite or potassium nitrite in the presence of aqueous hydrochloric or hydrobromic acids and then reacting with an iron(II) or iron(III) compound, optionally in the presence of additional amounts of hydrogen chloride or hydrogen bromide or alkali metal or alkaline earth metal chlorides or bromides.

Claims (36)

1. A process for preparing a compound of formula (II)

in which

X is chlorine or bromine,

R 1 , R 2 and R 3 are the same or different and are independently hydrogen, halogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, optionally substituted C 3 -C 6 -cycloalkyl or C 4 -C 6 -cycloalkenyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, optionally substituted phenyl, phenoxy, heterocyclyl or hetaryl, or cyano, C 1 -C 6 -alkylamino or di(C 1 -C 6 -alkyl)amino,

R 4 is halogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -alkynyl, C 2 -C 6 alkynyl, optionally substituted C 3 -C 6 -cycloalkyl or C 4 -C 6 -cycloalkenyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, optionally substituted phenyl, phenoxy, heterocyclyl or hetaryl, or cyano, C 1 -C 6 -alkylamino or di(C 1 -C 6 -alkyl)amino, and

n is 0, 1 or 2, characterized in that a compound of the formula (I):

in which R 1 , R 2 , R 3 , R 4 and n are each as defined above,

is diazotized by means of sodium nitrite or potassium nitrite in the presence of aqueous hydrochloric acid or hydrobromic acid, and then converted by addition of a substoichiometric amount of an iron(II) or iron(III) compound and optionally additional amounts of hydrogen chloride or hydrogen bromide or an alkali metal or alkaline earth metal chloride or bromide.

2. The process for preparing the compound of formula (II) according to claim 1 , in which

X is chlorine or bromine,

R 1 , R 2 and R 3 are the same or different and are independently hydrogen, halogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, optionally substituted C 3 -C 6 -cycloalkyl or C 4 -C 6 -cycloalkenyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, optionally substituted phenyl, phenoxy, heterocyclyl or hetaryl, or cyano, C 1 -C 6 -alkylamino or di(C 1 -C 6 -alkyl)amino,

R 4 is halogen, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, C 2 -C 6 -alkenyl, C 2 -C 6 -alkynyl, optionally substituted C 3 -C 6 -cycloalkyl or C 4 -C 6 -cycloalkenyl, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, optionally substituted phenyl, phenoxy, heterocyclyl or hetaryl, or cyano, C 1 -C 6 -alkylamino or di(C 1 -C 6 -alkyl)amino, and n is 0 or 1.

3. The process for preparing the compound of formula (II) according to claim 1 , in which

X is chlorine or bromine,

R 1 , R 2 and R 3 are the same or different and are independently hydrogen, fluorine, chlorine, bromine, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, optionally substituted cyclopropyl or cyclopentyl, C 1 -C 4 -alkoxy, optionally substituted phenyl or phenoxy, or cyano,

R 4 is fluorine, chlorine, bromine, C 1 -C 4 -alkyl, C 2 -C 4 -alkenyl, C 2 -C 4 -alkynyl, optionally substituted cyclopropyl or cyclopentyl, C 1 -C 4 -alkoxy, optionally substituted phenyl or phenoxy, or cyano, and

n is 0.

4. The process for preparing the compound of formula (II) according to claim 1 , in which

X is chlorine or bromine,

R 1 , R 2 and R 3 are the same or different and are independently hydrogen, chlorine, bromine, methyl, ethyl, i-propyl, n-propyl or cyclopropyl,

R 4 is chlorine, bromine, methyl, ethyl, i-propyl, n-propyl or cyclopropyl, and

n is 0 or 1.

5. The process for preparing the compound of formula (II) according to claim 1 , in which

X is chlorine or bromine,

R 1 is C 1 -C 4 -alkyl,

R 2 is hydrogen, C 1 -C 4 -alkyl or halogen,

R 3 is hydrogen or C 1 -C 4 -alkyl, and

n is 0.

6. The process according to claim 1 , characterized in that the iron(II) or iron(III) compound is used in amounts of 0.01 to 1 mol per mole of aniline of the formula (I).

7. The process according to claim 1 , characterized in that the iron(II) or iron(III) compound is used in amounts of 0.05 to 0.75 mol per mole of aniline of the formula (I).

8. The process according to claim 1 , characterized in that the iron compound used is iron(II) sulphate, iron(III) sulphate, iron(II) chloride, iron(III) chloride, iron(II) bromide, iron(III) bromide, iron(II) fluoride, iron(III) fluoride, iron(II) acetate, iron(II) propionate, iron(II) stearate, iron(II) sulphamate, iron(II) oxalate, iron(III) oxalate, iron(III) citrate, iron(II) gluconate, iron(II) acetylacetonate, iron(III) acetylacetonate, iron(III) nitrate, iron(III) phosphate, ammonium iron(II) sulphate, ammonium iron(III) sulphate, iron(II,III) oxide, iron(III) oxide or, where they exist, the particular hydrates thereof.

9. The process according to claim 8 , characterized in that the iron compound used is iron(II) sulphate, iron(III) sulphate, iron(II) chloride, iron(II) chloride, iron(II) bromide, iron(III) bromide or, where they exist, the particular hydrates thereof.

10. The process according to claim 1 , characterized in that an alkali metal or alkaline earth metal chloride or bromide is used in the second step.

11. The process according to claim 10 , characterized in that lithium chloride, sodium chloride, potassium chloride, magnesium chloride, calcium chloride, lithium bromide, sodium bromide, potassium bromide or magnesium bromide is used.

12. The process according to claim 1 , characterized in that hydrogen chloride or hydrogen bromide is used in the second step.

13. The process according to any one of claim 1 to 5 or 6 - 12 , wherein copper salts are not used.

Assignments (4)
NUNC PRO TUNC ASSIGNMENT Recorded Jul 4, 2023
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
Reel/Frame 064198/0823 →
CHANGE OF ADDRESS Recorded Jun 12, 2023
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 064021/0344 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 23, 2015
From: BAYER CROPSCIENCE AG
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 035009/0538 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 17, 2010
From: HIMMLER, THOMAS, DR.
To: BAYER CROPSCIENCE AG
Reel/Frame 024393/0664 →