WO2020212163A1 - Specific dehydrogenation process (i) - Google Patents

Specific dehydrogenation process (i) Download PDF

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Publication number
WO2020212163A1
WO2020212163A1 PCT/EP2020/059477 EP2020059477W WO2020212163A1 WO 2020212163 A1 WO2020212163 A1 WO 2020212163A1 EP 2020059477 W EP2020059477 W EP 2020059477W WO 2020212163 A1 WO2020212163 A1 WO 2020212163A1
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WO
WIPO (PCT)
Prior art keywords
formula
compound
compounds
process according
present
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/EP2020/059477
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English (en)
French (fr)
Inventor
Werner Bonrath
Marc-André Mueller
Bettina Wuestenberg
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
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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 JP2021556320A priority Critical patent/JP2022529573A/ja
Priority to BR112021020268-4A priority patent/BR112021020268B1/pt
Priority to US17/603,114 priority patent/US11851402B2/en
Priority to EP20714639.0A priority patent/EP3956304B1/en
Priority to CN202080028170.4A priority patent/CN113677662B/zh
Publication of WO2020212163A1 publication Critical patent/WO2020212163A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/32—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with formation of free hydrogen
    • C07C5/327—Formation of non-aromatic carbon-to-carbon double bonds only
    • 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
    • C07C403/12—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 esterified 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
    • C07C403/14—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 doubly-bound oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C5/00—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms
    • C07C5/42—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor
    • C07C5/44—Preparation of hydrocarbons from hydrocarbons containing the same number of carbon atoms by dehydrogenation with a hydrogen acceptor with halogen or a halogen-containing compound as an acceptor
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/02—Preparation of carboxylic acid esters by interreacting ester groups, i.e. transesterification
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/44—Preparation of carboxylic acid esters by oxidation-reduction of aldehydes, e.g. Tishchenko reaction
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/12—Acetic acid esters
    • C07C69/14—Acetic acid esters of monohydroxylic compounds
    • C07C69/145—Acetic acid esters of monohydroxylic compounds of unsaturated alcohols
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/22—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety
    • C07C69/24—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen having three or more carbon atoms in the acid moiety esterified with monohydroxylic compounds
    • 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

  • the present invention relates to a new dehydrogenation process.
  • the new dehydrogenation process according to the invention is a dehydrogenation of the following compounds of formula (I)
  • the two dehydrogenation products are those of formula (lla) and (Mb)
  • R’ has the same meaning as defined above.
  • the compound of formula (I) as well as of formula (II) can have any possible stereoisomeric form. Due to the 3 or 4 C-C-double bonds, there is variety of stereoisomeric forms. For the present invention the stereochemistry of the compounds of formula (I) and (II) is not essential.
  • the compound of formula (Mb) is an important intermediate in organic synthesis (especially in the synthesis of vitamin A and/or its derivatives).
  • This process is easy to handle, and it allows to provide a possibility to shorten the synthesis of vitamin A (and its derivatives).
  • the process of the present invention is carried out in the presence of at least one specific oxidative reactant.
  • the oxidative reactant used in the process of the present invention has the following formula (III)
  • Ri is -CN, -Cl or -F
  • R 2 is -CN, -Cl or -F
  • R 4 IS -H, -CHs, -Cl or -F.
  • the present invention relates to a process (P) for the production of the compounds of formula (II)
  • R has the same meanings as in the compound of formula (II), wherein the dehydrogenation is carried out in the presence of at least one oxidative reactant of formula (III)
  • Ri is -CN, -Cl or -F
  • R 2 is -CN, -Cl or F
  • R 4 is -H, -CHs, -Cl or -F.
  • Preferred oxidative reactants of formula (III) are those of the following formula (Ilia), (lllb) and (lllc):
  • the present invention relates to a process (P1 ) for the production of the compounds of formula (II), which is process (P), wherein the oxidative reactant is chosen from the group consisting of the compounds of formula (Ilia), (lllb) and (lllc)
  • the present invention relates to a process (P2) for the production of the compounds of formula (II), which is process (P), wherein the oxidative reactant is the compound of formula (lllc).
  • the amount of the oxidative reactant of formula (III) used in the process according to the present invention can vary.
  • the amount of the oxidative reactant of formula (III) usually goes from 0.5 mol-equivalent up to 5 mol-equivalent (in relation to compound of formula (II)). Preferably from 1 to 3 mol-equivalent (in relation to compound of formula (II)).
  • the present invention relates to a process (P2’) for the production of the compounds of formula (II), which is process (P2), wherein the amount of the oxidative reactant of formula (III) goes from 0.5 mol-equivalent up to 5 mol- equivalent (in relation to compound of formula (II)).
  • the present invention relates to a process (P2”) for the production of the compounds of formula (II), which is process (P2), wherein the amount of the oxidative reactant of formula (III) goes from 1 to 3 mol-equivalent (in relation to compound of formula (II)).
  • the process according to the present invention can also be carried out in the presence of at least one additive compound.
  • This additive compound is usually chosen from the group consisting of pyridine, butylhydroxyltoluol, hydroquinone and triethoxyamine.
  • the additive compound(s) is (are) added in amount of 0.001 - 1 mol-equivalent (in relation to compound of formula (II)), preferably 0.003 - 1 mol-equivalent (in relation to compound of formula (II)).
  • the present invention relates to a process (P3) for the production of the compounds of formula (II), which is process (P), (P1 ), (P2), (P2’) or (P2”), wherein the process is carried out in the presence of at least one additive compound.
  • the present invention relates to a process (P3’) for the production of the compounds of formula (II), which is process (P3), wherein the additive compound is chosen from the group consisting of pyridine, butylhydroxyltoluol, hydroquinone and triethoxyamine.
  • the present invention relates to a process (P3”) for the production of the compounds of formula (II), which is process (P3) or (P3’), wherein the additive compound is added in amount of 0.001 - 1 mol-equivalent (in relation to compound of formula (II)).
  • the present invention relates to a process (P3’”) for the production of the compounds of formula (II), which is process (P3) or (P3’), wherein the additive compound is added in amount of 0.003 - 1 mol-equivalent (in relation to compound of formula (II)).
  • the reaction is usually carried out in an inert solvent.
  • the solvent is usually an aromatic hydrocarbon such as benzene or toluol. Therefore, the present invention relates to a process (P4) for the production of the compounds of formula (II), which is process (P), (P1 ), (P2), (P2’), (P2”), (P3), (P3’), (P3”) or (P3’”), wherein the process is carried out in the presence of at least one inert solvent.
  • the present invention relates to a process (P4’) for the production of the compounds of formula (II), which is process (P4), wherein the solvent is an aromatic solvent.
  • the present invention relates to a process (P4”) for the production of the compounds of formula (II), which is process (P4), wherein the solvent is chosen from the group consisting of benzene and toluol.
  • the process according to the present is usually carried out at elevated temperatures. Usually the process according to the present invention is carried out at a temperature of from 0°C - 120 °C, preferably from 5°C - 100°C.
  • the present invention relates to a process (P5) for the production of the compounds of formula (II), which is process (P), (P1 ), (P2), (P2’), (P2”), (P3), (P3’), (P3”), (P3’”), (P4), (P4’) or (P4”), wherein the process is carried out at a temperature of from 0°C - 120 °C.
  • the present invention relates to a process (P5’) for the production of the compounds of formula (II), which is process (P), (P1 ), (P2), (P2’), (P2”), (P3), (P3’), (P3”), (P3’”), (P4), (P4’) or (P4”), wherein the process is carried out at a temperature of from 5°C - 100°C.
  • the process according to the present invention is one important step in the synthesis of vitamin A (and/or its derivatives).
  • the following examples serve to illustrate the invention.
  • the temperature is given in °C and all percentages are related to the weight. Examples
  • 7,8-Dihydroretinylactate 150 mg, 1.0 eq
  • DDQ 1.0 eq
  • triethoxyamine 0.5 mol%
  • Example 4 7,8-Dihydroretinyl acetate (180 mg, 1.0 eq) were dissolved in ethylacetate (20 ml_) and DDQ (1.0 eq) and triethoxyamine (0.5 mol%) were added. The reaction mixture was stirred for 0.5 h at 77°C. The solution was filtered over a plug of silica and all volatiles were evaporated under reduced pressure. Purification by column chromatography afforded the desired product (74% yield).
  • 7,8-Dihydroretinyl acetate (181 mg, 1.0 eq) were dissolved in ethylacetate (5 ml_) and DDQ (1.0 eq) and triethoxyamine (0.5 mol%) were added. The reaction mixture was stirred for 0.5 h at room temperature and o.5 h at 77°C. The solution was filtered over a plug of silica and all volatiles were evaporated under reduced pressure. Purification by column chromatography afforded the desired product (75% yield).

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Steroid Compounds (AREA)
PCT/EP2020/059477 2019-04-15 2020-04-03 Specific dehydrogenation process (i) Ceased WO2020212163A1 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP2021556320A JP2022529573A (ja) 2019-04-15 2020-04-03 特定の脱水素化方法（ｉ）
BR112021020268-4A BR112021020268B1 (pt) 2019-04-15 2020-04-03 Processo de desidrogenação específico (i)
US17/603,114 US11851402B2 (en) 2019-04-15 2020-04-03 Specific dehydrogenation process (I)
EP20714639.0A EP3956304B1 (en) 2019-04-15 2020-04-03 Specific dehydrogenation process (i)
CN202080028170.4A CN113677662B (zh) 2019-04-15 2020-04-03 特定的脱氢方法(i)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP19169206.0 2019-04-15
EP19169206 2019-04-15

Publications (1)

Publication Number Publication Date
WO2020212163A1 true WO2020212163A1 (en) 2020-10-22

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PCT/EP2020/059477 Ceased WO2020212163A1 (en) 2019-04-15 2020-04-03 Specific dehydrogenation process (i)

Country Status (5)

Country Link
US (1) US11851402B2 (https=)
EP (1) EP3956304B1 (https=)
JP (1) JP2022529573A (https=)
CN (1) CN113677662B (https=)
WO (1) WO2020212163A1 (https=)

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4825006A (en) * 1985-01-10 1989-04-25 Kuraray Co., Ltd. Process for producing vitamin A or its carboxylic acid esters, and intermediate compounds useful for the process

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1254613B (de) * 1966-05-17 1967-11-23 Basf Ag Verfahren zur Herstellung von Vitamin A-Aldehyd
JPS6289657A (ja) * 1985-10-16 1987-04-24 Kuraray Co Ltd ビタミンａ又はそのカルボン酸エステルの製造方法
JP6064264B2 (ja) * 2011-12-27 2017-01-25 ディーエスエム アイピー アセッツ ビー．ブイ． ビタミンａ中間体の触媒合成
BR112015027922B1 (pt) * 2013-05-08 2021-02-02 Dsm Ip Assets B.V processo de produção de acetato de dehidrolinalil (ii)

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4825006A (en) * 1985-01-10 1989-04-25 Kuraray Co., Ltd. Process for producing vitamin A or its carboxylic acid esters, and intermediate compounds useful for the process

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
L. DUHAMEL, ET AL.: "The OSM (oxidation state modification) concept: application to a new and rapid synthesis of retinoids", TETRAHEDRON LETTERS, vol. 35, no. 8, 21 February 1994 (1994-02-21), Elsevier Science Publishers, Oxford, GB, XP000426183, ISSN: 0040-4039, DOI: 10.1016/0040-4039(94)88025-5 *
LAW, WING C. ET AL., JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 110, no. 17, 1988, pages 5915 - 5917
O.O. TUTORSKAYA, ET AL.: "Synthetic investigations in the chemistry of polyene compounds. LII. Synthesis of retinoic and dihydroretinoic esters by the Reformatskii reaction", JOURNAL OF ORGANIC CHEMISTRY OF THE USSR, vol. 27, no. 7, July 1991 (1991-07-01), Consultants Bureau, New York, NY, US, pages 1237 - 1240, XP055698496, ISSN: 0022-3271 *
O.O.TUTORSKAYA ET AL., ZH.ORG.I KHIM., vol. 27, 1991, pages 1414
W.C. LAW, ET AL.: "The necessity of an intact polyene for the biological isomerisation of vitamin A", JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, vol. 110, no. 17, August 1988 (1988-08-01), American Chemical Society, Washington, DC, US, pages 5915 - 5917, XP055698570, ISSN: 0002-7863, DOI: 10.1021/ja00225a062 *

Also Published As

Publication number Publication date
US11851402B2 (en) 2023-12-26
US20220194891A1 (en) 2022-06-23
CN113677662A (zh) 2021-11-19
JP2022529573A (ja) 2022-06-23
CN113677662B (zh) 2024-07-16
EP3956304B1 (en) 2026-03-25
EP3956304A1 (en) 2022-02-23
BR112021020268A2 (pt) 2021-12-07

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