US20170305828A1 - Process for the preparation of 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone - Google Patents

Process for the preparation of 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone Download PDF

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US20170305828A1
US20170305828A1 US15/516,087 US201515516087A US2017305828A1 US 20170305828 A1 US20170305828 A1 US 20170305828A1 US 201515516087 A US201515516087 A US 201515516087A US 2017305828 A1 US2017305828 A1 US 2017305828A1
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Helmars Smits
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/004—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with organometalhalides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/45—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by condensation
    • C07C45/46—Friedel-Crafts reactions
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
    • C07C45/63—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by introduction of halogen; by substitution of halogen atoms by other halogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
    • C07C49/76—Ketones containing a keto group bound to a six-membered aromatic ring
    • C07C49/80—Ketones containing a keto group bound to a six-membered aromatic ring containing halogen

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  • the present invention relates to the preparation of 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone using 5-bromo-1,2,3-trichloro-benzene as a starting material.
  • 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone is an important intermediate for the preparation of pesticidally active isoxazoline-substituted benzamides as for example disclosed in EP 1932836A1.
  • 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone can be advantageously prepared by using 5-bromo-1,2,3-trichloro-benzene as a starting material.
  • 5-bromo-1,2,3-trichloro-benzene can be prepared as described in Narander, N.; Srinivasu, P.; Kulkarni, S.J.; Raghavan, K.V. Synth. Comm. 2000, 30, 3669 and Sott, R.; Hawner, C.; Johansen, J.E. Tetrahedron 2008, 64, 4135.
  • 3-Trifluoromethyl chalcones can be prepared according to methods disclosed in WO 2009/126668.
  • aryltrifluoromethyl ketones by reacting derivatives of trifluoroacetic acid with organometallic reagents derived from haloarenes is well known and for example described in WO 2012/120135 for the preparation of 2,2,2-trifluoro-1-(3,4,5-trichlorophenyl)ethanone.
  • organometallic reagents derived from haloarenes for example described in WO 2012/120135 for the preparation of 2,2,2-trifluoro-1-(3,4,5-trichlorophenyl)ethanone.
  • 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone the corresponding starting material is 5-bromo-1,3-dichloro-2-fluoro-benzene.
  • the process according to the invention is characterized by a reduced number of reaction steps and high selectivity and yield.
  • R 1 is C 1 -C 4 alkyl
  • M 2 is Lithium or Magnesium
  • X is halogen or absent; with a compound of formula IV
  • R 2 is halogen, hydroxyl, C 1 -C 4 alkoxy, (di-C 1 -C 4 alkyl)amino, OC(O)CF 3 , phenoxy or OM 1 ; wherein M 1 is
  • alkyl groups occurring in the definitions of the substituents can be straight-chain or branched and are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl or tert-butyl.
  • Alkoxy is, for example, methoxy, ethoxy, propoxy, i-propoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy.
  • the compound of formula V can be prepared by reacting a compound of formula II first with magnesium then with a compound of formula IV
  • R 2 is halogen, hydroxyl, C 1 -C 4 alkoxy, (di-C 1 -C 4 alkyl)amino, OC(O )CF 3 , phenoxy or OM 1 ; wherein M 1 is Lithium, Magnesium, Sodium or Potassium;.
  • the compound of formula V can be prepared by reacting a compound of formula II first with an organometallic reagent of formula III
  • R 1 is C 1 -C 4 alkyl
  • M 2 is Lithium or Magnesium
  • R 2 is halogen, hydroxyl, C 1 -C 4 alkoxy, (di-C 1 -C 4 alkyl)amino, OC(O)CF 3 , phenoxy or OM 1 ; wherein M 1 is Lithium, Magnesium, Sodium or Potassium.
  • the compound of formula III is preferably used in form of a complex with LiCl.
  • Suitable solvents include but are not limited to organic ethers such as tetrahydrofuran, 2-methyl-tetrahydrofuran, 1,4-dioxane, diethyl ether, t-butylmethyl ether and hydrocarbons such as toluene, benzene, hexane and cyclohexane.
  • the reaction can be carried out at a temperature from ⁇ 80° C. to 50° C., preferably from ⁇ 20° C. to 25° C.
  • the compound of formula I can be prepared by reaction of a compound of formula V with an alkali metalfluoride in the presence of a phase transfer catalyst.
  • Suitable metal fluorides include KF, LiF and NaF.
  • Suitable phase transfer catalysts include phosphonium salts of general formula (R 3 ) 4 PX and ammonium salts of general formula (R 3 ) 4 NX where R 3 is C 1 -C 4 alkyl or phenyl and X is halogen. Phosphonium salts are preferred.
  • Suitable solvents are polar in nature and include, but are not limited to sulfolane, dimethylformamide and dimethylsulfoxide.
  • the reaction can be carried out at a temperature from 100° C. to 250° C., preferably from 120° C. to 160° C.
  • R 1 is C 1 -C 4 alkyl
  • M 2 is Lithium or Magnesium
  • X is halogen or absent; with a compound of formula IV
  • R 2 is halogen, hydroxyl, C 1 C 4 alkoxy, (di-C 1 -C 4 alkyl)amino, OC(O)CF 3 , phenoxy or OM 1 ;
  • M 1 is Lithium, Magnesium, Sodium or Potassium
  • the organometallic reagent is isopropylmagnesiumchloride complexed with LiCl.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

The invention relates to a process for the preparation of a compound of formula I comprising a) reacting a compound of formula II in the presence of magnesium or an organometallic reagent of formula III R1M2X (III), wherein R1 is CI-C4alkyl; M2 is Li or Mg and X is halogen or absent; with a compound of formula IV CF3-C(O)-R2 (IV), wherein R2 is halogen, hydroxyl, CI-C4alkoxy, (di-CI-C4alkyl)amino, OC(O)CF3, phenoxy or OM1; wherein M1 is Lithium, Magnesium, Sodium or Potassium; to a compound of formula V, and b) reacting the compound of formula V with alkali metal fluoride in the presence of catalytic amounts of a phase transfer catalyst in the presence of a polar solvent to the compound of formula I.
Figure US20170305828A1-20171026-C00001

Description

  • The present invention relates to the preparation of 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone using 5-bromo-1,2,3-trichloro-benzene as a starting material.
  • 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone is an important intermediate for the preparation of pesticidally active isoxazoline-substituted benzamides as for example disclosed in EP 1932836A1.
  • 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone can be advantageously prepared by using 5-bromo-1,2,3-trichloro-benzene as a starting material. 5-bromo-1,2,3-trichloro-benzene can be prepared as described in Narander, N.; Srinivasu, P.; Kulkarni, S.J.; Raghavan, K.V. Synth. Comm. 2000, 30, 3669 and Sott, R.; Hawner, C.; Johansen, J.E. Tetrahedron 2008, 64, 4135. 3-Trifluoromethyl chalcones can be prepared according to methods disclosed in WO 2009/126668.
  • The synthesis of aryltrifluoromethyl ketones by reacting derivatives of trifluoroacetic acid with organometallic reagents derived from haloarenes is well known and for example described in WO 2012/120135 for the preparation of 2,2,2-trifluoro-1-(3,4,5-trichlorophenyl)ethanone. For the synthesis of 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone the corresponding starting material is 5-bromo-1,3-dichloro-2-fluoro-benzene. However, this substance is difficult to prepare in particular on a large scale with the only described synthesis being an inefficient multistep approach described in Miller, M.W.; Mylari, B.L.; Howes, H.L.; Figdor, S.K.; Lynch, M.J.; Lynch, J.E.; Koch, R.C. J. Med. Chem. 1980, 23, 1083, CN 101177379, WO 2009/070485 and CN 103664511 (Scheme 1).
  • Figure US20170305828A1-20171026-C00002
  • Therefore, it is highly desirable to prepare 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone from the more easily accessible 2,2,2-trifluoro-1-(3,4,5-trichlorophenyl)ethanone. Surprisingly, it was found that reacting 2,2,2-trifluoro-1-(3,4,5-trichlorophenyl)ethanone with potassium fluoride in the presence of a phase transfer catalyst and a polar solvent provided the desired 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone. trifluoro-ethanone. While such nucleophilic aromatic substitution reactions are well known for nitroaromatic compounds (as for example disclosed in WO 92/00270) there is no prior art describing comparable reactions with trifluoromethyl ketones since this group is in general not known to be a sufficiently strong activating group.
  • It is therefore the object of the present invention to provide a process for the preparation of 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone using 5-bromo-1,2,3-trichloro-benzene as an intermediate. The process according to the invention is characterized by a reduced number of reaction steps and high selectivity and yield.
  • Thus, according to the present invention, there is provided a process for the preparation of the compound of formula I
  • Figure US20170305828A1-20171026-C00003
  • comprising
    a) reacting the compound of formula II
  • Figure US20170305828A1-20171026-C00004
  • in the presence of magnesium or an organometallic reagent of formula III

  • R1—M2X  (III),
  • wherein
    R1 is C1-C4alkyl;
    • M2 is Lithium or Magnesium and
  • X is halogen or absent;
    with a compound of formula IV

  • CF3—C(O)—R2  (IV),
  • wherein
    R2 is halogen, hydroxyl, C1-C4alkoxy, (di-C1-C4alkyl)amino, OC(O)CF3, phenoxy or OM1; wherein M1 is
    • Lithium, Magnesium, Sodium or Potassium;
  • to the compound of formula V,
  • Figure US20170305828A1-20171026-C00005
  • and
    b) reacting the compound of formula V with an alkali metal fluoride in the presence of catalytic amounts of a phase transfer catalyst in the presence of a polar solvent to the compound of formula I.
  • The alkyl groups occurring in the definitions of the substituents can be straight-chain or branched and are, for example, methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, iso-butyl or tert-butyl. Alkoxy is, for example, methoxy, ethoxy, propoxy, i-propoxy, n-butoxy, isobutoxy, sec-butoxy and tert-butoxy. The following scheme describes the reactions of the invention in more detail.
  • Figure US20170305828A1-20171026-C00006
    • Step a)
  • The compound of formula V can be prepared by reacting a compound of formula II first with magnesium then with a compound of formula IV

  • CF3—C(O)R2  (IV),
  • wherein R2 is halogen, hydroxyl, C1-C4alkoxy, (di-C1-C4alkyl)amino, OC(O )CF3, phenoxy or OM1; wherein M1 is Lithium, Magnesium, Sodium or Potassium;. Alternatively, the compound of formula V can be prepared by reacting a compound of formula II first with an organometallic reagent of formula III

  • R1—M2X  (III),
  • wherein
    R1 is C1-C4alkyl;
    • M2 is Lithium or Magnesium and
  • X is halogen or absent; and then with the compound of formula IV

  • CF3—C(O)R2  (IV),
  • wherein R2 is halogen, hydroxyl, C1-C4alkoxy, (di-C1-C4alkyl)amino, OC(O)CF3, phenoxy or OM1; wherein M1 is Lithium, Magnesium, Sodium or Potassium. The compound of formula III is preferably used in form of a complex with LiCl.
  • Typically the reaction is performed in an aprotic organic solvent. Suitable solvents include but are not limited to organic ethers such as tetrahydrofuran, 2-methyl-tetrahydrofuran, 1,4-dioxane, diethyl ether, t-butylmethyl ether and hydrocarbons such as toluene, benzene, hexane and cyclohexane. The reaction can be carried out at a temperature from −80° C. to 50° C., preferably from −20° C. to 25° C.
    • Step b):
  • The compound of formula I can be prepared by reaction of a compound of formula V with an alkali metalfluoride in the presence of a phase transfer catalyst. Suitable metal fluorides include KF, LiF and NaF. Suitable phase transfer catalysts include phosphonium salts of general formula (R3)4PX and ammonium salts of general formula (R3)4NX where R3 is C1-C4alkyl or phenyl and X is halogen. Phosphonium salts are preferred.
  • Typically the reaction is performed in an organic solvent or mixtures thereof. Suitable solvents are polar in nature and include, but are not limited to sulfolane, dimethylformamide and dimethylsulfoxide.
  • The reaction can be carried out at a temperature from 100° C. to 250° C., preferably from 120° C. to 160° C.
  • A preferred embodiment of the process of the invention comprising
  • a) reacting the compound of formula II
  • Figure US20170305828A1-20171026-C00007
  • in the presence of an organometallic reagent of formula III

  • R1—M2X  (III),
  • wherein
    R1 is C1-C4alkyl;
    • M2 is Lithium or Magnesium and
  • X is halogen or absent;
    with a compound of formula IV

  • CF3—C(O)—R2  (IV),
  • wherein R2 is halogen, hydroxyl, C1C4alkoxy, (di-C1-C4alkyl)amino, OC(O)CF3, phenoxy or OM1; wherein
    • M1 is Lithium, Magnesium, Sodium or Potassium;
  • to the compound of formula V,
  • Figure US20170305828A1-20171026-C00008
  • and
    b) reacting the compound of formula V with metal fluoride selected from KF, LiF and NaF in the presence of catalytic amounts of a phase transfer catalyst selected from the group consisting of phosphonium salts of general formula (R3)4PX and ammonium salts of general formula (R3)4NX wherein R3 is C1-C4alkyl or phenyl and X is halogen; in the presence of a polar solvent selected from the group consisting of sulfolane, dimethylformamide and dimethylsulfoxide, to the compound of formula I. In said preferred embodiment of the invention, the organometallic reagent is isopropylmagnesiumchloride complexed with LiCl.
    • PREPARATORY EXAMPLES Example 1: Preparation of 2,2,2-trifluoro-1-(3,4,5-trichlorophenyl)ethanone of Formula V
  • Figure US20170305828A1-20171026-C00009
  • To a solution of 5-bromo-1,2,3-trichloro-benzene (220 g, 811 mmol) in tetrahydrofuran (1600 ml) was added 1.3 M iPrMgCl.LiCl in THF (1250 ml, 1622 mmol) slowly at 20° C. The reaction mixture was stirred for 2 hours and cooled to 0° C. Methyl 2,2,2-trifluroacetate (314.8 g, 2434 mmol) was added slowly and the reaction mixture was stirred at ambient temperature for 1 hour. The reaction mixture was cooled to 0° C. and 2.0 M HCl (810 ml, 1622 mmol) was added dropwise during 30 min. The resulting mixture was diluted with ethyl acetate, the organic layer was washed with brine, dried over anhydrous MgSO4 and evaporated under reduced pressure. The crude product was dissolved in a minimum amount of cyclohexane and the solution was cooled to −10° C. The formed precipitate was filtered off to afford 2,2,2-trifluoro-1-(3,4,5-trichlorophenyl)ethanone (122 g) as a yellow solid. The filtrate was diluted with cyclohexane and washed twice with acetonitrile. Cyclohexane phase was evaporated under reduced pressure and the residue was dissolved in a minimum amount of cyclohexane. The solution was cooled to −10° C. and another portion of 2,2,2-trifluoro-1-(3,4,5-trichlorophenyl)ethanone (35 g) was filtered off. 1H NMR (400 MHz, CDCl3) δ8.07-8.05 (m, 2H).
    • Example 2: Preparation of 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone of formula I
  • Figure US20170305828A1-20171026-C00010
  • To a solution of 2,2,2-trifluoro-1-(3,4,5-trichlorophenypethanone (1.0 g, 3.6 mmol) in sulfolane (3 ml) was added dry potassium fluoride (0.35 g, 4.32 mmol) and tetraphenylphosphonium bromide (0.015 g, 0.036 mmol). The resulting reaction mixture was stirred at 160° C. for 5 hours. The reaction mixture was distilled under reduced pressure. Fractions containing the product were further purified with silica gel chromatography (eluting with pure heptane) to afford 1-(3,5-dichloro-4-fluoro-phenyl)-2,2,2-trifluoro-ethanone (0.571 g) as a colorless oil and a mixture of ketone and hydrate forms (ca 3:1). 19F NMR (400 MHz, CDCl3) δ−71.5, −84.7, −102.4, −112.9.

Claims (8)

1. A process for the preparation of the compound of formula I
Figure US20170305828A1-20171026-C00011
comprising
a) reacting the compound of formula II
Figure US20170305828A1-20171026-C00012
in the presence of magnesium or an organometallic reagent of formula III

R1—M2X  (III),
wherein
R1 is C1-C4alkyl;
M2 is Lithium or Magnesium and
X is halogen or absent;
with a compound of formula IV

CF3—C(O)—R2  (IV),
wherein R2 is halogen, hydroxyl, C1-C4alkoxy, (di-C1-C4alkyl)amino, OC(O)CF3, phenoxy or 0M1; wherein
M1 is Lithium, Magnesium, Sodium or Potassium;
to the compound of formula V,
Figure US20170305828A1-20171026-C00013
and
b) reacting the compound of formula V with an alkali metal fluoride in the presence of catalytic amounts of a phase transfer catalyst in the presence of a polar solvent to the compound of formula I.
2. A process according to claim 1, comprising
a) reacting the compound of formula II
Figure US20170305828A1-20171026-C00014
in the presence of an organometallic reagent of formula III

R1—M2X  (III)
wherein
R1 is C1-C4alkyl;
M2 is Lithium or Magnesium and
X is halogen or absent.
3. A process according to claim 2, wherein the organometallic reagent is isopropylmagnesiumchloride complexed with LiCl.
4. A process according to claim 1, wherein the alkali metal fluoride is selected from KF, LiF and NaF.
5. A process according to claim 1, wherein the phase transfer catalyst is selected from the group consisting of phosphonium salts of general formula (R3)4PX and ammonium salts of general formula (R3)4NX wherein R3 is C1-C4alkyl or phenyl and X is halogen.
6. A process according to claim 1, wherein the polar solvent is selected from the group consisting of sulfolane, dimethylformamide and dimethylsulfoxide.
7. A process according to claim 1, comprising
a) reacting the compound of formula II
Figure US20170305828A1-20171026-C00015
in the presence of an organometallic reagent of formula III

R1—M2X  (III)
wherein
R1 is C1-C4alkyl;
M2 is Lithium or Magnesium and
X is halogen or absent;
with a compound of formula IV

CF3—C(O)—R2  (IV),
wherein R2 is halogen, hydroxyl, C1-C4alkoxy, (di-C1-C4alkyl)amino, OC(O)CF3, phenoxy or OM1; wherein
M1 is Lithium, Magnesium, Sodium or Potassium;
to the compound of formula V,
Figure US20170305828A1-20171026-C00016
and
b) reacting the compound of formula V with an alkali metal fluoride selected from KF, LiF and NaF in the presence of catalytic amounts of a phase transfer catalyst selected from the group consisting of phosphonium salts of general formula (R3)4PX and ammonium salts of general formula (R3)4NX wherein R3 is C1-C4alkyl or phenyl and X is halogen; in the presence of a polar solvent selected from the group consisting of sulfolane, dimethylformamide and dimethylsulfoxide, to the compound of formula I.
8. A process according to claim 7, wherein the organometallic reagent is isopropylmagnesiumchloride complexed with LiCl.
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