[go: up one dir, main page]

SG11201608429TA - Synthesis of r-glucosides, sugar alcohols, reduced sugar alcohols, and furan derivatives of reduced sugar alcohols - Google Patents

Synthesis of r-glucosides, sugar alcohols, reduced sugar alcohols, and furan derivatives of reduced sugar alcohols

Info

Publication number
SG11201608429TA
SG11201608429TA SG11201608429TA SG11201608429TA SG11201608429TA SG 11201608429T A SG11201608429T A SG 11201608429TA SG 11201608429T A SG11201608429T A SG 11201608429TA SG 11201608429T A SG11201608429T A SG 11201608429TA SG 11201608429T A SG11201608429T A SG 11201608429TA
Authority
SG
Singapore
Prior art keywords
sugar alcohols
reduced sugar
glucosides
synthesis
reduced
Prior art date
Application number
SG11201608429TA
Inventor
Kenneth Stensrud
chi-cheng Ma
Kevin Martin
Original Assignee
Archer Daniels Midland Co
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 Archer Daniels Midland Co filed Critical Archer Daniels Midland Co
Publication of SG11201608429TA publication Critical patent/SG11201608429TA/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/34Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D307/38Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/40Radicals substituted by oxygen atoms
    • C07D307/42Singly bound oxygen atoms
    • C07D307/44Furfuryl alcohol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/02Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
    • C07D307/04Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • C07D307/10Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having no double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D307/12Radicals substituted by oxygen atoms
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/38Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals
    • B01J23/40Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of noble metals of the platinum group metals
    • B01J23/46Ruthenium, rhodium, osmium or iridium
    • B01J23/462Ruthenium
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/72Copper
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J25/00Catalysts of the Raney type
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/02Sulfur, selenium or tellurium; Compounds thereof
    • B01J27/053Sulfates
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/14Phosphorus; Compounds thereof
    • B01J27/16Phosphorus; Compounds thereof containing oxygen, i.e. acids, anhydrides and their derivates with N, S, B or halogens without carriers or on carriers based on C, Si, Al or Zr; also salts of Si, Al and Zr
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J27/00Catalysts comprising the elements or compounds of halogens, sulfur, selenium, tellurium, phosphorus or nitrogen; Catalysts comprising carbon compounds
    • B01J27/20Carbon compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/60Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by elimination of -OH groups, e.g. by dehydration
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/18Polyhydroxylic acyclic alcohols
    • C07C31/22Trihydroxylic alcohols, e.g. glycerol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/18Polyhydroxylic acyclic alcohols
    • C07C31/24Tetrahydroxylic alcohols, e.g. pentaerythritol
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07GCOMPOUNDS OF UNKNOWN CONSTITUTION
    • C07G3/00Glycosides
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02EREDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
    • Y02E50/00Technologies for the production of fuel of non-fossil origin
    • Y02E50/10Biofuels, e.g. bio-diesel

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Saccharide Compounds (AREA)
  • Furan Compounds (AREA)
  • Catalysts (AREA)
SG11201608429TA 2014-04-10 2014-04-10 Synthesis of r-glucosides, sugar alcohols, reduced sugar alcohols, and furan derivatives of reduced sugar alcohols SG11201608429TA (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US2014/033581 WO2015156803A1 (en) 2014-04-10 2014-04-10 Synthesis of r-glucosides, sugar alcohols, reduced sugar alcohols, and furan derivatives of reduced sugar alcohols

Publications (1)

Publication Number Publication Date
SG11201608429TA true SG11201608429TA (en) 2016-11-29

Family

ID=54288223

Family Applications (1)

Application Number Title Priority Date Filing Date
SG11201608429TA SG11201608429TA (en) 2014-04-10 2014-04-10 Synthesis of r-glucosides, sugar alcohols, reduced sugar alcohols, and furan derivatives of reduced sugar alcohols

Country Status (10)

Country Link
US (2) US20170029393A1 (en)
EP (1) EP3129341A4 (en)
JP (1) JP6449907B2 (en)
KR (1) KR20160146787A (en)
CN (1) CN106458805B (en)
AU (1) AU2014390020A1 (en)
CA (1) CA2945298C (en)
RU (1) RU2016141809A (en)
SG (1) SG11201608429TA (en)
WO (1) WO2015156803A1 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017070071A1 (en) * 2015-10-20 2017-04-27 Shell Oil Company Process for the production of glycols
ES2924952T3 (en) * 2018-04-13 2022-10-11 Archer Daniels Midland Co Conversion of 1,2,5,6-hexanetetrol (HTO) to tetrahydrofuranedicarboxylic acid (THFDCA)
CN113563398B (en) * 2021-06-30 2023-10-13 渭南师范学院 Method for synthesizing alkyl glycoside by cascade catalysis of straw
CN114906841B (en) * 2022-06-23 2023-10-17 上海海事大学 Preparation method of amorphous nano carbon particle/graphene aerogel composite material

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4820880A (en) * 1987-05-18 1989-04-11 Michigan Biotechnology Institute Process for the production of 3,4-dideoxyhexitol
IT1249318B (en) * 1991-05-23 1995-02-22 Zambon Spa BENZOTIAZEPINE PREPARATION PROCESS FOR CYCLING WITH PHOSPHONIC ACIDS
JPH08291159A (en) * 1995-04-25 1996-11-05 Mitsui Toatsu Chem Inc Method for producing 3- (hydroxymethyl) tetrahydrofuran
JPH09301967A (en) * 1996-05-14 1997-11-25 Kuraray Co Ltd Production of 3-hydroxymethyltetrahydrofuran
JP2007145736A (en) * 2005-11-25 2007-06-14 Canon Inc Manufacturing method of 5-hydroxymethylfurfural
EP2390247A1 (en) * 2010-05-26 2011-11-30 Netherlands Organisation for Scientific Research (Advanced Chemical Technologies for Sustainability) Preparation of caprolactone, caprolactam, 2,5-tetrahydrofuran dimethanol, 1,6-hexanediol or 1,2,6-hexanetriol from 5-hydroxymethyl-2-furfuraldehyde
CN101948451B (en) * 2010-08-18 2013-03-06 南京威尔化工有限公司 Preparation method of high-purity 1,4-sorbitan
WO2013102002A1 (en) * 2011-12-28 2013-07-04 E. I. Du Pont De Nemours And Company Processes for making furfurals
KR101421514B1 (en) * 2012-05-22 2014-07-30 대구가톨릭대학교산학협력단 Method for preparing isosorbide from sorbitol using water-compatible lewis acid
WO2015156806A1 (en) * 2014-04-10 2015-10-15 Archer Daniels Midland Company Synthesis of r-glucosides, sugar alcohols, reduced sugar alcohols, and furan derivatives of reduced sugar alcohols
EP3131413A4 (en) * 2014-04-10 2017-08-30 Archer-Daniels-Midland Company Synthesis of reduced sugar alcohols, furan derivatives

Also Published As

Publication number Publication date
US20180258059A1 (en) 2018-09-13
JP2017517491A (en) 2017-06-29
CA2945298A1 (en) 2015-10-15
EP3129341A4 (en) 2017-12-06
JP6449907B2 (en) 2019-01-09
US10519124B2 (en) 2019-12-31
WO2015156803A1 (en) 2015-10-15
CN106458805B (en) 2019-10-25
KR20160146787A (en) 2016-12-21
US20170029393A1 (en) 2017-02-02
RU2016141809A (en) 2018-05-10
CA2945298C (en) 2021-05-25
EP3129341A1 (en) 2017-02-15
CN106458805A (en) 2017-02-22
AU2014390020A1 (en) 2016-10-27

Similar Documents

Publication Publication Date Title
IL255266A0 (en) Amido-substituted cyclohexane derivatives
SG11201706729SA (en) Derivatives of sobetirome
SG11201608426PA (en) Synthesis of reduced sugar alcohols, furan derivatives
EP3114107A4 (en) Propellane derivates and synthesis
PL2913319T3 (en) Synthesis of guerbet alcohols
IL251607A0 (en) Low bitter chicory products
EP3160970A4 (en) Synthesis of halichondrin analogs and uses thereof
PT3283171T (en) Derivatives of amphotericin b
ZA201607198B (en) Low ph synthesis of zinc-lysine complex
GB201406977D0 (en) Fluoroalkylfluorene derivatives
EP3391446A4 (en) Selective oxidation of furan based alcohols via electro-generative process
SG11201606662QA (en) Method for synthesis of a biopolymer derivative, a biopolymer derivative and its use
AP2016009545A0 (en) Naphthyridinedione derivatives
EP3242554A4 (en) Concise synthesis of urea derivatives of amphotericin b
EP3129343A4 (en) Synthesis of shorter chain polyols
AP2016009530A0 (en) Cycloalkyl-linked diheterocycle derivatives
RS59218B1 (en) Novel cyp-eicosanoid derivatives
SG11201608429TA (en) Synthesis of r-glucosides, sugar alcohols, reduced sugar alcohols, and furan derivatives of reduced sugar alcohols
IL247531A0 (en) Hexose derivatives, preparation and uses thereof
PL3174849T3 (en) Synthesis of pyrrolidine derivatives
IL243185A0 (en) Spectral sensing of ablation
GB201705849D0 (en) Synthesis of chirally enriched 2,4-distributed tetrahydropyran-4-OL and its derivatives
EP3206695A4 (en) Scalable synthesis of reduced toxicity derivative of amphotericin b
GB201410779D0 (en) Barometer clock
HUE057149T2 (en) Micromolecule compound, method of synthesis and application thereof