WO2013182607A1 - Process for the production of 4-alkanoyloxy-2-methylbutanoic acid - Google Patents

Process for the production of 4-alkanoyloxy-2-methylbutanoic acid Download PDF

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Publication number
WO2013182607A1
WO2013182607A1 PCT/EP2013/061605 EP2013061605W WO2013182607A1 WO 2013182607 A1 WO2013182607 A1 WO 2013182607A1 EP 2013061605 W EP2013061605 W EP 2013061605W WO 2013182607 A1 WO2013182607 A1 WO 2013182607A1
Authority
WO
WIPO (PCT)
Prior art keywords
formula
compound
process according
transition metal
metal salt
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/EP2013/061605
Other languages
English (en)
French (fr)
Inventor
Werner Bonrath
Jan SCHÜTZ
Bettina WÜSTENBERG
Thomas Netscher
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
DSM IP Assets BV
Original Assignee
DSM IP Assets BV
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by DSM IP Assets BV filed Critical DSM IP Assets BV
Priority to US14/401,868 priority Critical patent/US9447017B2/en
Priority to CN201380029603.8A priority patent/CN104350036B/zh
Priority to JP2015515511A priority patent/JP6209776B2/ja
Priority to EA201401323A priority patent/EA026148B1/ru
Priority to IN9213DEN2014 priority patent/IN2014DN09213A/en
Priority to EP13728998.9A priority patent/EP2855418B1/en
Priority to ES13728998.9T priority patent/ES2643221T3/es
Priority to KR1020147034114A priority patent/KR102100521B1/ko
Publication of WO2013182607A1 publication Critical patent/WO2013182607A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/28—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/29—Preparation of carboxylic acid esters by modifying the hydroxylic moiety of the ester, such modification not being an introduction of an ester group by introduction of oxygen-containing functional groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/15—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of oxides of carbon exclusively
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
    • C07C403/06—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms
    • C07C403/08—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by singly-bound oxygen atoms by hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C403/00—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone
    • C07C403/24—Derivatives of cyclohexane or of a cyclohexene or of cyclohexadiene, having a side-chain containing an acyclic unsaturated part of at least four carbon atoms, this part being directly attached to the cyclohexane or cyclohexene or cyclohexadiene rings, e.g. vitamin A, beta-carotene, beta-ionone having side-chains substituted by six-membered non-aromatic rings, e.g. beta-carotene
    • 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
    • C07C45/008—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reaction with tri- or tetrahalomethyl compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
    • C07C51/21—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen
    • C07C51/23—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups
    • C07C51/245—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with molecular oxygen of oxygen-containing groups to carboxyl groups of keto groups or secondary alcohol groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D311/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings
    • C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
    • C07D311/58—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4
    • C07D311/70—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring other than with oxygen or sulphur atoms in position 2 or 4 with two hydrocarbon radicals attached in position 2 and elements other than carbon and hydrogen in position 6
    • C07D311/72—3,4-Dihydro derivatives having in position 2 at least one methyl radical and in position 6 one oxygen atom, e.g. tocopherols
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2523/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00
    • C07C2523/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group C07C2521/00 of the iron group metals or copper
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00—Systems containing only non-condensed rings
    • C07C2601/12—Systems containing only non-condensed rings with a six-membered ring
    • C07C2601/16—Systems containing only non-condensed rings with a six-membered ring the ring being unsaturated

Definitions

  • isoprene isoterpene
  • ⁇ - carotene or other carotenoids e.g. canthaxanthin, zeaxanthin or astaxanthin
  • vitamin E or vitamin A as well as other structurally similar compounds.
  • Isoprene which has the following chemical structure is an important chemical unit for a group of chemical compounds known as isopre- noids.
  • Carotenoids as well as vitamin E as mentioned above are i.e. such isopre- noids.
  • R signifies a C1-C15 alkyl moiety or a C2-C18 alkenyl moiety, is an important compound (building block, starting compound) in such organic synthesis (for the production of isoprenoids).
  • R is a C1-C15 alkyl moiety
  • the alkyl moiety is linear.
  • Especially preferred alkyl moieties are methyl, ethyl and pentadecyl.
  • R is a C2-C18 alkenyl moiety
  • the alkenyl moiety is unbranched.
  • the goal of the present invention was to provide an improved process of production of compounds of formula (I).
  • R signifies a C1-C15 alkyl moiety or a C2-C18 alkenyl moiety
  • the present invention relates to a process of production of a compound of formula (I)
  • R signifies a C1-C15 alkyl moiety or a C2-C18 alkenyl
  • At least one transition metal salt is used as a catalyst.
  • the present invention relates to a process of production of a compound of formula (I)
  • R signifies a linear C1-C15 alkyl moiety (preferably methyl, ethyl and penta- decyl),
  • At least one transition metal salt is used as a catalyst.
  • transition metaf is defined as any element in the d-block of the periodic table, which includes groups 3 to 12 on the periodic table.
  • the f-block is also (in the form of the lanthanide and actinide se- ries) part of the definition.
  • the transition metal is the cation of the salt and the anion can be organic as well inorganic.
  • Preferred transition metals are Cu, Co, Fe and Cr.
  • the anion of the transition metal salt is not crucial for the invention. Any usually used anion can be the counterion. Preferred anions are halides (such as CI “ , Br “ or I " ), PO 4 3" , SO 4 2" or O(CO)CH 3 ).
  • Preferred salts are Co(O(CO)CH 3 ) 2 , Cu(O(CO)CH 3 ) 2 , CoSO 4 , CuSO 4 , Fe 2 (SO 4 ) 3 , CoCI 2 , CuCI 2 and FeCI 3 .
  • the present invention relates to a preferred process of production of a compound of formula (I)
  • R signifies a C1-C15 alkyl moiety or a C2-C18 alkenyl moiety
  • At least one transition metal salt selected from the group consisting of Co(O(CO)CH 3 ) 2 , Cu(O(CO)CH 3 ) 2 , CoSO 4 , CuSO 4 , Fe 2 (SO 4 ) 3 , CoCI 2 , CuCI 2 and FeCb is used as a catalyst.
  • the present invention relates to a preferred process of production of a compound of formula (la)
  • At least one transition metal salt selected from the group consisting of Co(O(CO)CH 3 ) 2 , Cu(O(CO)CH 3 ) 2 , CoSO 4 , CuSO 4 , Fe 2 (SO 4 ) 3 , CoCI 2 , CuCI 2 and FeCb is used as a catalyst.
  • the present invention also relates to a preferred process of production of a compound of formula (lb)
  • At least one transition metal salt selected from the group consisting of Co(O(CO)CH 3 ) 2 , Cu(O(CO)CH 3 ) 2 , CoSO 4 , CuSO 4 , Fe 2 (SO 4 ) 3 , CoCI 2 , CuCI 2 and FeCI 3 is used as a catalyst.
  • the present invention also relates to a preferred process of production of a compound of formula (lc) wherein a compound of formula (lie)
  • At least one transition metal salt selected from the group consisting of Co(O(CO)CH 3 ) 2 , Cu(O(CO)CH 3 ) 2 , CoSO 4 , CuSO 4 , Fe 2 (SO 4 ) 3 , C0CI2, CuCI 2 and FeCb is used as a catalyst.
  • the process of the present invention is a catalytic oxidation.
  • the oxidant used in the process is a gas comprising 0 2 . It can be pure O 2 gas as well as a mixture which comprises O 2 (such e.g. air).
  • the process according to the present invention is carried by using air as oxidant.
  • the process according to the present invention can be carried under pressure (up to 20bar) as well as at ambient pressure.
  • Preferably the process according to the present invention is carried out ambient pressure.
  • the transition metal salt catalyst (as well as a mixture of such salts) is used in catalytic amounts.
  • the transition metal salt catalyst (as well as a mixture of such salts) is used in an amount of 0.0005 - 0.1 mol equivalent (related to the mol of compound of formula (II)). Therefore the present invention relates to a preferred process of production of a compound of formula (la)
  • the present invention also relates to a preferred process of production of a compound of formula (lb)
  • the present invention also relates to a preferred process of production of a compound of formula (Ic)
  • the process according to present invention is usually carried out at temperatures of -10°C - 150°C, preferably 0°C - 80°C, more preferably 15°C - 70°C.
  • the process according to the present invention is usually carried out in a polar apro- tic or polar protic solvent, as well as in mixtures of such solvents.
  • Suitable solvents are esters (such as ethyl acetate), carbonates (such as ethylene carbonate), car- boxylic acids (such as acetic acid, formic acid), alcohols (such methanol, ethanol, propanol, isopropanol), DMSO, DMF, acetone, dichloroethane, dichloromethane and chloroform.
  • the compound of formula (I) is used in the synthesis of an intermediate, which is then used for the synthesis of vitamin E, vitamin A or ⁇ -carotene, can- thaxanthin, zeaxanthin or astaxanthin. Such process are known from the prior art.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Catalysts (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
PCT/EP2013/061605 2012-06-05 2013-06-05 Process for the production of 4-alkanoyloxy-2-methylbutanoic acid Ceased WO2013182607A1 (en)

Priority Applications (8)

Application Number Priority Date Filing Date Title
US14/401,868 US9447017B2 (en) 2012-06-05 2013-06-05 Process for the production of 4-alkanoyloxy-2-methylbutanoic acid
CN201380029603.8A CN104350036B (zh) 2012-06-05 2013-06-05 4‑烷酰氧基‑2‑甲基丁酸的生产方法
JP2015515511A JP6209776B2 (ja) 2012-06-05 2013-06-05 ４−アルカノイルオキシ−２−メチルブタン酸の製造方法
EA201401323A EA026148B1 (ru) 2012-06-05 2013-06-05 Способ получения 4-алканоилокси-2-метилбутановой кислоты
IN9213DEN2014 IN2014DN09213A (enExample) 2012-06-05 2013-06-05
EP13728998.9A EP2855418B1 (en) 2012-06-05 2013-06-05 Process for the production of 4-alkanoyloxy-2-methylbutanoic acid
ES13728998.9T ES2643221T3 (es) 2012-06-05 2013-06-05 Proceso para la producción de ácido 4-alcanoiloxi-2-metilbutanoico
KR1020147034114A KR102100521B1 (ko) 2012-06-05 2013-06-05 4-알칸오일옥시-2-메틸부탄산의 제조 방법

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP12170781 2012-06-05
EP12170781.4 2012-06-05

Publications (1)

Publication Number Publication Date
WO2013182607A1 true WO2013182607A1 (en) 2013-12-12

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ID=48626428

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Application Number Title Priority Date Filing Date
PCT/EP2013/061605 Ceased WO2013182607A1 (en) 2012-06-05 2013-06-05 Process for the production of 4-alkanoyloxy-2-methylbutanoic acid

Country Status (9)

Country Link
US (1) US9447017B2 (enExample)
EP (1) EP2855418B1 (enExample)
JP (1) JP6209776B2 (enExample)
KR (1) KR102100521B1 (enExample)
CN (1) CN104350036B (enExample)
EA (1) EA026148B1 (enExample)
ES (1) ES2643221T3 (enExample)
IN (1) IN2014DN09213A (enExample)
WO (1) WO2013182607A1 (enExample)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109609758B (zh) * 2018-12-29 2022-02-18 江苏雄风科技有限公司 一种低氯离子高纯硫酸钴的萃取洗涤方法
JP2023506710A (ja) * 2019-12-23 2023-02-20 ディーエスエム アイピー アセッツ ビー．ブイ． １，３－α－ジエン（ＩＩ）の官能化

Citations (1)

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Publication number Priority date Publication date Assignee Title
US4665091A (en) * 1985-11-04 1987-05-12 Merck & Co., Inc. Macrocyclic lactone HMG-CoA reductase inhibitors

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DE1918694C3 (de) * 1969-04-12 1974-07-04 Basf Ag, 6700 Ludwigshafen Verfahren zur Herstellung von Carbonsäureestern des 3-Formylbutanol-(l) durch die Oxo-Synthese
US4500727A (en) * 1981-03-23 1985-02-19 Kuraray Co., Ltd. Process for producing methyl lactate
JPS57156442A (en) * 1981-03-23 1982-09-27 Kuraray Co Ltd Preparation of methyl lactate
JPS58140038A (ja) * 1982-02-16 1983-08-19 Kuraray Co Ltd アゼライン酸の製造法
US4668699A (en) * 1985-08-05 1987-05-26 Merck & Co., Inc. Novel HMG-CoA reductase inhibitors
JPH04198149A (ja) * 1990-11-29 1992-07-17 Mitsui Toatsu Chem Inc ２―クロロプロピオンアルデヒドの酸化方法
JP3756537B2 (ja) * 1994-11-16 2006-03-15 株式会社クラレ ジメチルデカンジアールおよびその製造方法
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CN101391948B (zh) * 2007-09-20 2012-06-13 浙江新和成股份有限公司 3-甲基-2-丁烯酸的制备方法
JP2011246426A (ja) * 2010-05-31 2011-12-08 Mitsubishi Chemicals Corp ホルミルアシロキシアルカン及び環状エーテルの製造方法
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BASSAM EL ALI ET AL: "FORMIC ACID-PALLADIUM ACETATE-1,4-BIS(DIPHENYLPHOSPHINO)BUTANE: AN EFFECTIVE CATALYTIC SYSTEM FOR REGIOSELECTIVE HYDROCARBOXYLATION OF SIMPLE AND FUNCTIONALIZED OLEFINS", JOURNAL OF MOLECULAR CATALYSIS, ELSEVIER, NL, vol. 77, no. 1, 1 January 1992 (1992-01-01), pages 7 - 13, XP009052481, ISSN: 0304-5102, DOI: 10.1016/0304-5102(92)80179-K *
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Also Published As

Publication number Publication date
US20150099894A1 (en) 2015-04-09
US9447017B2 (en) 2016-09-20
CN104350036A (zh) 2015-02-11
ES2643221T3 (es) 2017-11-21
JP2015520177A (ja) 2015-07-16
JP6209776B2 (ja) 2017-10-11
EA026148B1 (ru) 2017-03-31
EP2855418A1 (en) 2015-04-08
EP2855418B1 (en) 2017-08-09
CN104350036B (zh) 2017-05-17
EA201401323A1 (ru) 2015-03-31
KR102100521B1 (ko) 2020-04-14
IN2014DN09213A (enExample) 2015-07-10
KR20150016544A (ko) 2015-02-12

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