IE47102B1 - Method of preparing ascorbic acid and intermediates specially adapted for use therein - Google Patents

Method of preparing ascorbic acid and intermediates specially adapted for use therein

Info

Publication number
IE47102B1
IE47102B1 IE1103/78A IE110378A IE47102B1 IE 47102 B1 IE47102 B1 IE 47102B1 IE 1103/78 A IE1103/78 A IE 1103/78A IE 110378 A IE110378 A IE 110378A IE 47102 B1 IE47102 B1 IE 47102B1
Authority
IE
Ireland
Prior art keywords
lactone
carbon atoms
alkyl
aldehyde
hydroxyl
Prior art date
Application number
IE1103/78A
Other languages
English (en)
Other versions
IE781103L (en
Original Assignee
Pfizer
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=25185352&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IE47102(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Pfizer filed Critical Pfizer
Publication of IE781103L publication Critical patent/IE781103L/xx
Publication of IE47102B1 publication Critical patent/IE47102B1/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
    • C07D307/26Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D307/30Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/32Oxygen atoms
    • C07D307/33Oxygen atoms in position 2, the oxygen atom being in its keto or unsubstituted enol form
    • 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
    • C07D307/56Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D307/62Three oxygen atoms, e.g. ascorbic acid
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/04Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/02Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains two hetero rings
    • C07D493/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F7/00Compounds containing elements of Groups 4 or 14 of the Periodic Table
    • C07F7/02Silicon compounds
    • C07F7/08Compounds having one or more C—Si linkages
    • C07F7/18Compounds having one or more C—Si linkages as well as one or more C—O—Si linkages
    • C07F7/1804Compounds having Si-O-C linkages
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07HSUGARS; DERIVATIVES THEREOF; NUCLEOSIDES; NUCLEOTIDES; NUCLEIC ACIDS
    • C07H7/00Compounds containing non-saccharide radicals linked to saccharide radicals by a carbon-to-carbon bond
    • C07H7/02Acyclic radicals
    • C07H7/027Keto-aldonic acids
    • 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
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Biotechnology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Biochemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Molecular Biology (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Furan Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
IE1103/78A 1977-06-03 1978-06-01 Method of preparing ascorbic acid and intermediates specially adapted for use therein IE47102B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US05/803,020 US4111958A (en) 1977-06-03 1977-06-03 Ascorbic acid synthesis

Publications (2)

Publication Number Publication Date
IE781103L IE781103L (en) 1978-12-03
IE47102B1 true IE47102B1 (en) 1983-12-28

Family

ID=25185352

Family Applications (1)

Application Number Title Priority Date Filing Date
IE1103/78A IE47102B1 (en) 1977-06-03 1978-06-01 Method of preparing ascorbic acid and intermediates specially adapted for use therein

Country Status (7)

Country Link
US (1) US4111958A (en, 2012)
EP (1) EP0000092B1 (en, 2012)
JP (2) JPS5845432B2 (en, 2012)
DE (1) DE2860636D1 (en, 2012)
DK (1) DK248178A (en, 2012)
IE (1) IE47102B1 (en, 2012)
IT (1) IT1098308B (en, 2012)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4232168A (en) * 1977-06-13 1980-11-04 Pfizer Inc. Preparation of ascorbic acid intermediates
US4283340A (en) * 1977-06-13 1981-08-11 Pfizer Inc. Ascorbic acid intermediates
US4421924A (en) * 1980-05-05 1983-12-20 Pfizer Inc. Ascorbic acid intermediates and their preparation
JPS57501581A (en, 2012) * 1980-08-14 1982-09-02
US4423236A (en) * 1980-08-14 1983-12-27 National Foundation For Cancer Research, Inc. 5,6,-0-Isoalkylidene ascorbic acid derivatives
US4552888A (en) * 1982-01-15 1985-11-12 Eli Lilly And Company Ascorbic acid ethers in angiogene
DK36784A (da) * 1983-02-25 1984-08-26 Hoffmann La Roche Fremgangsmaade til fremstilling af chirale aldehyder
US4931558A (en) * 1983-09-21 1990-06-05 Eli Lilly And Company Processes for preparing intermediates of picenadol
JPS61192907U (en, 2012) * 1985-05-24 1986-12-01
JPS6244712U (en, 2012) * 1985-09-09 1987-03-18
JPS63114705U (en, 2012) * 1987-01-20 1988-07-23
US4845246A (en) * 1987-06-15 1989-07-04 Takeda Chemical Industries, Ltd. Ascorbic acid ester
US5569875A (en) * 1992-03-16 1996-10-29 Legend Products Corporation Methods of making explosive compositions, and the resulting products
US5442079A (en) * 1993-05-10 1995-08-15 Virginia Polytechnic Institute And State University Method for preparing erythruronolactone
FR2761991B1 (fr) 1997-04-11 1999-06-25 Ceca Sa 5-6,o alkylidenes gluconolactones-1(4) et derives, procedes de preparation et utilisations
US6610863B2 (en) 2000-12-22 2003-08-26 Eastman Chemical Company Continuous process for producing L-ascorbic acid
DE10231890B4 (de) * 2002-07-12 2004-07-01 Basf Ag Verfahren zur Abtrennung von Ascorbinsäure aus einem polaren, Ascorbinsäure und 2-Keto-L-gulonsäure enthaltenden Lösungsmittel
KR101630654B1 (ko) * 2012-07-20 2016-06-15 후지필름 가부시키가이샤 에칭방법, 이것을 사용한 반도체 기판 제품 및 반도체 소자의 제조방법

Also Published As

Publication number Publication date
JPS5719117B2 (en, 2012) 1982-04-20
IT7824178A0 (it) 1978-06-02
JPS543058A (en) 1979-01-11
EP0000092B1 (en) 1981-04-29
JPS5845432B2 (ja) 1983-10-08
US4111958A (en) 1978-09-05
JPS55149286A (en) 1980-11-20
IE781103L (en) 1978-12-03
EP0000092A1 (en) 1978-12-20
DE2860636D1 (en) 1981-08-06
IT1098308B (it) 1985-09-07
DK248178A (da) 1978-12-04

Similar Documents

Publication Publication Date Title
EP0000092B1 (en) Method of preparing ascorbic acid and intermediates specially adapted for use therein
Hanessian et al. Synthesis of (+)-avermectin B1a
US5625078A (en) Processes for the production of 13-ether derivatives of milbemycins and novel intermediates therefor
KR101682058B1 (ko) 카르바모일피리돈 hiv 인테그라제 억제제를 위한 제조방법 및 중간체
EP0141057B1 (en) Novel 4'-demethyl-4-epipodophyllotoxin derivatives, a process for their preparation and their use as medicaments
Just et al. C-Nucleosides and related compounds. XV. The synthesis of D, L-2′-epi-showdomycin and D, L-showdomycin
Jacobi et al. Bis heteroannulation. 1. Model studies in the synthesis of highly oxygenated sesquiterpenes
Van den Ouweland et al. Synthesis of 3, 5‐Dihydroxy‐2‐Methyl‐5, 6‐Dihydropyran‐4‐one from Aldohexoses and Secondary Amine salts
Gypser et al. D-Erythronolactone as a C 4 building unit. Part 2.1 A short and efficient synthesis of both enantiomers of epi-muricatacin, a diastereoisomer of the native acetogenin from Annona muricata
Grieco et al. Ring-fluorinated prostaglandins: total synthesis of (.+-.)-10. alpha.-fluoroprostaglandin F2. alpha. methyl ester
US4232168A (en) Preparation of ascorbic acid intermediates
Sarabia-García et al. Unstabilized diazo derivatives from carbohydrates. Application to the synthesis of 2-deamino-tunicamine and products related to C-disaccharides
US4421924A (en) Ascorbic acid intermediates and their preparation
US4283340A (en) Ascorbic acid intermediates
David et al. Some derivatives of 3-deoxy-D-glycero-D-galacto-non-2-ulosonic acid (KDN)
SU1698253A1 (ru) Способ получени производных гексагидро-5-гидрокси-4-гидроксиметил-2Н-циклопента( @ )-фуран-2-она
KR0171410B1 (ko) 10-(2-프로피닐)에스트르-4-엔-3,17-디온의 제조방법
Alzérreca et al. Orientational effect of the phenylsulfonyl group in the thermal spiroketalization of dihydroxyketone equivalents
Horneman et al. Highly Functionalised Cyclopentanes by Radical Cyclisation of Unsaturated Bromolactones III. Preparation of Carbaaldohexofuranoses. Determination of the Relative Configuration at C-4/C-5 of 2, 3-Unsaturated Heptono-1, 4-lactones by Means of 1H NMR Spectroscopy
WO2020169643A1 (en) DIETHYLAMINE SALT OF 3α-TETRAHYDROPYRANYLOXY-6α-ETHYL-7α-HYDROXY-5ß-CHOLANIC ACID
Szechner et al. Total synthesis of protected form of fungi metabolite cortalcerone
SU1038341A1 (ru) Способ получени @ -арилиндолотриметинцианинов
JPH03123780A (ja) 2H―ベンゾ[b]キノリジン誘導体
CN120271545A (zh) 一种二苯并-α-吡喃酮类化合物的合成方法及其应用
Honda et al. MMMSMMMM Op? OR? основn