FR3135978B1 - Synthese de l’acide levulinique par hydratation d’alcool furfurylque en presence d’un catalyseur homogene acide et d’un solvant a base d’ether et/ou d’acetals - Google Patents

Synthese de l’acide levulinique par hydratation d’alcool furfurylque en presence d’un catalyseur homogene acide et d’un solvant a base d’ether et/ou d’acetals Download PDF

Info

Publication number
FR3135978B1
FR3135978B1 FR2205180A FR2205180A FR3135978B1 FR 3135978 B1 FR3135978 B1 FR 3135978B1 FR 2205180 A FR2205180 A FR 2205180A FR 2205180 A FR2205180 A FR 2205180A FR 3135978 B1 FR3135978 B1 FR 3135978B1
Authority
FR
France
Prior art keywords
hydration
synthesis
ether
furfuryl alcohol
acetals
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.)
Active
Application number
FR2205180A
Other languages
English (en)
Other versions
FR3135978A1 (fr
Inventor
Pierre-Alain Breuil
Kim Larmier
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.)
IFP Energies Nouvelles IFPEN
Original Assignee
IFP Energies Nouvelles IFPEN
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 IFP Energies Nouvelles IFPEN filed Critical IFP Energies Nouvelles IFPEN
Priority to FR2205180A priority Critical patent/FR3135978B1/fr
Priority to PCT/EP2023/062616 priority patent/WO2023232427A1/fr
Priority to US18/869,867 priority patent/US20250353806A1/en
Publication of FR3135978A1 publication Critical patent/FR3135978A1/fr
Application granted granted Critical
Publication of FR3135978B1 publication Critical patent/FR3135978B1/fr
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/42Separation; Purification; Stabilisation; Use of additives
    • C07C51/43Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation
    • C07C51/44Separation; Purification; Stabilisation; Use of additives by change of the physical state, e.g. crystallisation by distillation

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

La présente invention concerne un procédé de synthèse de l’acide lévulinique par l’hydratation d’alcool furfurylique à une température comprise entre 25 et 140°C en présence d’un catalyseur homogène acide et d’un solvant à base d’éther et/ou d’acétal. L’utilisation d’un tel solvant permet d’obtenir un rendement équivalent voir meilleur à ceux obtenus avec des solvants connus, tout en présentant des propriétés de stabilité importantes.
FR2205180A 2022-05-31 2022-05-31 Synthese de l’acide levulinique par hydratation d’alcool furfurylque en presence d’un catalyseur homogene acide et d’un solvant a base d’ether et/ou d’acetals Active FR3135978B1 (fr)

Priority Applications (3)

Application Number Priority Date Filing Date Title
FR2205180A FR3135978B1 (fr) 2022-05-31 2022-05-31 Synthese de l’acide levulinique par hydratation d’alcool furfurylque en presence d’un catalyseur homogene acide et d’un solvant a base d’ether et/ou d’acetals
PCT/EP2023/062616 WO2023232427A1 (fr) 2022-05-31 2023-05-11 Synthese de l'acide levulinique par hydratation d'alcool furfurylque en presence d'un catalyseur homogene acide et d'un solvant a base d'ether et/ou d'acetals
US18/869,867 US20250353806A1 (en) 2022-05-31 2023-05-11 Synthesis of levulinic acid by hydration of furfuryl alcohol in the presence of a homogeneous acid catalyst and of a solvent based on ether and/or acetals

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR2205180 2022-05-31
FR2205180A FR3135978B1 (fr) 2022-05-31 2022-05-31 Synthese de l’acide levulinique par hydratation d’alcool furfurylque en presence d’un catalyseur homogene acide et d’un solvant a base d’ether et/ou d’acetals

Publications (2)

Publication Number Publication Date
FR3135978A1 FR3135978A1 (fr) 2023-12-01
FR3135978B1 true FR3135978B1 (fr) 2025-02-28

Family

ID=82319932

Family Applications (1)

Application Number Title Priority Date Filing Date
FR2205180A Active FR3135978B1 (fr) 2022-05-31 2022-05-31 Synthese de l’acide levulinique par hydratation d’alcool furfurylque en presence d’un catalyseur homogene acide et d’un solvant a base d’ether et/ou d’acetals

Country Status (3)

Country Link
US (1) US20250353806A1 (fr)
FR (1) FR3135978B1 (fr)
WO (1) WO2023232427A1 (fr)

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2780588A (en) 1954-12-08 1957-02-05 Quaker Oats Co Stabilization of levulinic acid
US3752849A (en) 1970-03-18 1973-08-14 Otsuka Kagaku Yakuhin Manufacture of levulinic acid
FR2640263B1 (fr) 1988-12-09 1991-06-14 Organo Synthese Ste Fse Preparation d'acide levulinique
CN103209951B (zh) 2010-11-11 2016-04-20 赛格提斯公司 酮基羧酸、酮基羧酸酯、其制造和使用方法
US8389761B2 (en) 2011-05-25 2013-03-05 Wisconsin Alumni Research Foundation Method to produce and recover levulinic acid and/or gamma-valerolactone from aqueous solutions using alkylphenols
MX2016000623A (es) 2013-07-17 2016-05-26 Dsm Ip Assets Bv Proceso para aislar acido levulinico.
CN107867996B (zh) 2016-09-23 2021-02-09 中国石油化工股份有限公司 乙酰丙酸类化合物的分离方法
IT201700068744A1 (it) 2017-06-21 2018-12-21 Bio On Spa Processo per la produzione di acido levulinico.
CN116529232A (zh) * 2020-09-23 2023-08-01 博奥股份公司 用于生产乙酰丙酸的方法

Also Published As

Publication number Publication date
WO2023232427A1 (fr) 2023-12-07
FR3135978A1 (fr) 2023-12-01
US20250353806A1 (en) 2025-11-20

Similar Documents

Publication Publication Date Title
Gu et al. Heterogeneously catalyzed etherification of glycerol: new pathways for transformation of glycerol to more valuable chemicals
Egami et al. Product control in alkene trifluoromethylation: hydrotrifluoromethylation, vinylic trifluoromethylation, and iodotrifluoromethylation using Togni Reagent
Coulombel et al. Triflic acid-catalysed cyclisation of unsaturated alcohols
Toledo et al. Organocatalytic oxidation of aldehydes to mixed anhydrides
Hu et al. Simultaneous hydrogenation and acid-catalyzed conversion of the biomass-derived furans in solvents with distinct polarities
Takenaka et al. Synthesis of 2, 2-difluoro-homoallylic alcohols via ring-opening of gem-difluorocyclopropane and aerobic oxidation by photo-irradiation in the presence of an organic pigment
Chien et al. Photo-Fries rearrangement in flow under aqueous micellar conditions
KR102492874B1 (ko) 시클로부탄테트라카르복실산 유도체의 제조 방법
Mikhalchenko et al. A practical way to synthesize chiral fluoro-containing polyhydro-2H-chromenes from monoterpenoids
Dasgupta et al. Synthesis of chiral trifluoromethyl benzylamines by heterogeneous catalytic reductive amination
Márquez et al. Barbier-Type Diastereoselective Allylation of α-Amino Aldehydes with an Enantiopure 2-Sulfinylallyl Building Block
Liu et al. Enantioselective Michael Addition of Cyclohexanone to Nitroolefins Catalyzed by a New Pyrrolidinyl-isosteviol Bifunctional Organocatalyst in Water
Song et al. Functional ionic liquids as efficient and recyclable catalysts for the methylation of formaldehyde with aromatics
Esmaeilpour et al. 4-Dodecylbenzenesulfonic acid (DBSA): an efficient, eco-friendly and chemoselective catalyst for the synthesis of 1, 1-diacetates under solvent-free conditions at room temperature
Xu et al. Phosphite-catalyzed alkoxycarbonylation of aryl diazonium salts
EP0040400A1 (fr) Procédé de préparation d'éthers monoallyliques de pyrocatéchine
RU2852476C1 (ru) Способ получения альфа-ангелика лактона из левулиновой кислоты
US10550057B1 (en) Method of making a dialdeyhde
DE2306464B2 (de) Teilfluorierte Aminoäther und Verfahren zu ihrer Herstellung
JP7289119B2 (ja) 光学活性置換テトラヒドロフラン誘導体を合成する方法
FR3151851A1 (fr) Procede de preparation d’anhydride cyclique a partir d’une lactone
Scholten et al. A new allene hexamer
US8513467B2 (en) Production of 2,4-diones from 4-hydroxy-6-substituted-2-pyrones
Shendrik et al. Haloacrylic acids XI. Photochemical reactions of aliphatic aldehydes with methyl trifluoroacrylate
US3847952A (en) Process for producing alcohols of the furan series

Legal Events

Date Code Title Description
PLFP Fee payment

Year of fee payment: 2

PLSC Publication of the preliminary search report

Effective date: 20231201

PLFP Fee payment

Year of fee payment: 3

PLFP Fee payment

Year of fee payment: 4