CA2800797C - Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran-dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde - Google Patents

Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran-dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde Download PDF

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Publication number
CA2800797C
CA2800797C CA2800797A CA2800797A CA2800797C CA 2800797 C CA2800797 C CA 2800797C CA 2800797 A CA2800797 A CA 2800797A CA 2800797 A CA2800797 A CA 2800797A CA 2800797 C CA2800797 C CA 2800797C
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Canada
Prior art keywords
hexanediol
hexanetriol
catalyst
dimethanol
tetrahydrofuran
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CA2800797A
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English (en)
French (fr)
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CA2800797A1 (en
Inventor
Johannes Gerardus De Vries
Teddy
Pim Huat Phua
Ignacio Vladimiro Melian Cabrera
Hero Jan Heeres
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NEDERLANDSE ORGANISATIE VOOR WETENSCHAPPELIJK ONDERZOEK (NWO)
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NEDERLANDSE ORGANISATIE VOOR WETENSCHAPPELIJK ONDERZOEK (NWO)
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Publication of CA2800797A1 publication Critical patent/CA2800797A1/en
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
    • C07D313/02—Seven-membered rings
    • C07D313/04—Seven-membered rings not condensed with other rings
    • 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
    • C07C29/132—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 an oxygen containing functional group
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
    • C07D201/02—Preparation of lactams
    • C07D201/08—Preparation of lactams from carboxylic acids or derivatives thereof, e.g. hydroxy carboxylic acids, lactones or nitriles
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Catalysts (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)
  • Furan Compounds (AREA)
  • Pyrane Compounds (AREA)
CA2800797A 2010-05-26 2011-03-23 Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran-dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde Active CA2800797C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP10163881.5 2010-05-26
EP10163881A EP2390247A1 (en) 2010-05-26 2010-05-26 Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde
PCT/NL2011/050200 WO2011149339A1 (en) 2010-05-26 2011-03-23 Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran-dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde

Publications (2)

Publication Number Publication Date
CA2800797A1 CA2800797A1 (en) 2011-12-01
CA2800797C true CA2800797C (en) 2019-04-16

Family

ID=42797300

Family Applications (1)

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CA2800797A Active CA2800797C (en) 2010-05-26 2011-03-23 Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran-dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde

Country Status (8)

Country Link
US (1) US9199961B2 (https=)
EP (2) EP2390247A1 (https=)
JP (1) JP6327853B2 (https=)
CN (1) CN103228626B (https=)
BR (1) BR112012029996B1 (https=)
CA (1) CA2800797C (https=)
ES (1) ES2727436T3 (https=)
WO (1) WO2011149339A1 (https=)

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CN107074761B (zh) * 2014-10-30 2020-04-14 东丽株式会社 ε-己内酰胺的制造方法
JP2017537920A (ja) 2014-12-02 2017-12-21 レノビア インコーポレイテッド ５−ヒドロキシメチルフルフラールから２，５−ビスヒドロキシメチルフラン、２，５−ビス−ヒドロキシメチルテトラヒドロフラン、１，６−ヘキサンジオールおよび１，２，６−ヘキサントリオールを生成する工程
CN104591369A (zh) * 2014-12-23 2015-05-06 南京林业大学 一种用于促使过氧化氢产生羟基自由基的复合药剂及其应用
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CN106866360B (zh) * 2015-12-10 2020-09-04 中国科学院大连化学物理研究所 一种5-羟甲基糠醛催化转化制备1,6-己二醇的方法
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EP3652161A1 (en) 2017-07-12 2020-05-20 Stora Enso Oyj Purified 2,5-furandicarboxylic acid pathway products
CN111777578B (zh) * 2020-07-15 2022-06-24 烟台大学 5-羟甲基糠醛加氢制备2,5-二羟甲基四氢呋喃的方法
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KR20250076198A (ko) * 2023-11-22 2025-05-29 한국생산기술연구원 루테늄 담지 알루미나 촉매, 그의 제조방법 및 그를 이용한 연속식 테트라하이드로퓨란 다이메탄올(thfdm) 제조장치
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Also Published As

Publication number Publication date
JP6327853B2 (ja) 2018-05-23
WO2011149339A1 (en) 2011-12-01
BR112012029996B1 (pt) 2021-10-26
ES2727436T3 (es) 2019-10-16
JP2013531638A (ja) 2013-08-08
CN103228626A (zh) 2013-07-31
CN103228626B (zh) 2016-08-03
US9199961B2 (en) 2015-12-01
CA2800797A1 (en) 2011-12-01
US20130137863A1 (en) 2013-05-30
EP2576506A1 (en) 2013-04-10
EP2390247A1 (en) 2011-11-30
BR112012029996A2 (pt) 2021-05-04
EP2576506B1 (en) 2019-03-06

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