MX348375B - Produccion de propan-1,2-diol opticamente puro. - Google Patents

Produccion de propan-1,2-diol opticamente puro.

Info

Publication number
MX348375B
MX348375B MX2014000655A MX2014000655A MX348375B MX 348375 B MX348375 B MX 348375B MX 2014000655 A MX2014000655 A MX 2014000655A MX 2014000655 A MX2014000655 A MX 2014000655A MX 348375 B MX348375 B MX 348375B
Authority
MX
Mexico
Prior art keywords
diol
propane
optically pure
production
pure propane
Prior art date
Application number
MX2014000655A
Other languages
English (en)
Other versions
MX2014000655A (es
Inventor
Tietz Wolfgang
Schulze Joachim
Boerner Armin
Shuklov Ivan
Kühlein Klaus
Original Assignee
Thyssenkrupp Ind Solutions Ag
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 Thyssenkrupp Ind Solutions Ag filed Critical Thyssenkrupp Ind Solutions Ag
Publication of MX2014000655A publication Critical patent/MX2014000655A/es
Publication of MX348375B publication Critical patent/MX348375B/es

Links

Classifications

    • 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
    • C07C29/74—Separation; Purification; Use of additives, e.g. for stabilisation
    • 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
    • C07C29/136—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 of >C=O containing groups, e.g. —COOH
    • C07C29/147—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 of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof
    • C07C29/149—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 of >C=O containing groups, e.g. —COOH of carboxylic acids or derivatives thereof with hydrogen or hydrogen-containing gases
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B57/00—Separation of optically-active compounds
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C31/00—Saturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
    • C07C31/18—Polyhydroxylic acyclic alcohols
    • C07C31/20—Dihydroxylic alcohols
    • C07C31/205—1,3-Propanediol; 1,2-Propanediol
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P41/00—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture
    • C12P41/003—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions
    • C12P41/004—Processes using enzymes or microorganisms to separate optical isomers from a racemic mixture by ester formation, lactone formation or the inverse reactions by esterification of alcohol- or thiol groups in the enantiomers or the inverse reaction
    • C—CHEMISTRY; METALLURGY
    • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
    • C12P7/00—Preparation of oxygen-containing organic compounds
    • C12P7/02—Preparation of oxygen-containing organic compounds containing a hydroxy group
    • C12P7/04—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic
    • C12P7/18—Preparation of oxygen-containing organic compounds containing a hydroxy group acyclic polyhydric
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07—Optical isomers

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Wood Science & Technology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • Biotechnology (AREA)
  • Microbiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Biochemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • General Engineering & Computer Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Genetics & Genomics (AREA)
  • Analytical Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

La invención se refiere a un procedimiento para producir propano-1, 2- diolopticamente puro, que comprende las siguientes etapas de procedimiento: a. Hidrogenación de lactidas, en donde se lleva a cabo una catálisis heterogénea catalizada por metales en presencia de hidrogeno produciéndose un producto bruto que contiene propano-1,2-diol, y b. Resolución racémica cinetica dinámica, en que se produce propano-1,2-diol ópticamente puro dentro de un intervalo de >_ 99% de e.e.
MX2014000655A 2011-07-20 2012-06-22 Produccion de propan-1,2-diol opticamente puro. MX348375B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE102011107959A DE102011107959A1 (de) 2011-07-20 2011-07-20 Herstellung von optisch reinem Propan-1,2-diol
PCT/EP2012/002638 WO2013010618A1 (de) 2011-07-20 2012-06-22 Herstellung von optisch reinem propan-1,2-diol

Publications (2)

Publication Number Publication Date
MX2014000655A MX2014000655A (es) 2014-11-13
MX348375B true MX348375B (es) 2017-05-15

Family

ID=46458423

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2014000655A MX348375B (es) 2011-07-20 2012-06-22 Produccion de propan-1,2-diol opticamente puro.

Country Status (12)

Country Link
US (1) US20140212957A1 (es)
EP (1) EP2734488B1 (es)
KR (1) KR20140076548A (es)
CN (1) CN103781745B (es)
BR (1) BR112014001110A8 (es)
CA (1) CA2841089A1 (es)
CO (1) CO6890108A2 (es)
DE (1) DE102011107959A1 (es)
MX (1) MX348375B (es)
MY (1) MY165921A (es)
RU (1) RU2553262C1 (es)
WO (1) WO2013010618A1 (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2912882T3 (es) * 2014-11-18 2022-05-30 Archer Daniels Midland Co Procedimiento para preparar propilenglicol de origen biológico a partir de ésteres de ácido láctico
CN110256203B (zh) * 2019-06-05 2022-06-14 江苏扬农化工集团有限公司 一种环氧丙烷废水中缩合醇醚资源化利用的方法
CN118388317B (zh) * 2024-06-27 2024-09-06 潍坊汇韬化工有限公司 一种利用环氧丙烷制备丙二醇的方法

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100644165B1 (ko) * 2002-03-14 2006-11-10 학교법인 포항공과대학교 아미노시클로펜타디에닐 루테늄 촉매를 이용한 키랄화합물 분할 방법
KR20040099348A (ko) * 2002-03-22 2004-11-26 다우 글로벌 테크놀로지스 인크. 프로필렌 글리콜 알킬 (또는 아릴) 에테르 및 에테르아세테이트의 효소적 분할
GB0321240D0 (en) 2003-09-11 2003-10-08 Avecia Ltd Process
WO2006124899A2 (en) 2005-05-13 2006-11-23 Cargill, Incorporated Production of derivatives of lactide, production of lactides, and use of lactide in foods and to produce polymers
EP1970360B1 (en) 2007-03-16 2016-08-31 Takasago International Corporation Method for producing alcohols
JP5491854B2 (ja) * 2007-04-03 2014-05-14 株式会社カネカ 液相でラクトンおよびカルボン酸エステルを水素化するアルコール類の製造方法
EE200800009A (et) 2008-02-21 2009-10-15 Nordbiochem OÜ Katalsaator ja meetod hdrokskarbokslhapete estrite kataltiliseks redutseerimiseks glkoolideks
JP5477557B2 (ja) 2008-09-09 2014-04-23 高砂香料工業株式会社 エステル又はラクトン類の水素還元によるアルコール類の製造方法
EE200900073A (et) 2009-09-22 2011-06-15 Nordbiochem O� Katalsaator ja meetod hdrokskarbokslhapete estrite kataltiliseks hdrogeenimiseks glkoolideks

Also Published As

Publication number Publication date
WO2013010618A1 (de) 2013-01-24
DE102011107959A1 (de) 2013-01-24
CO6890108A2 (es) 2014-03-10
CN103781745B (zh) 2016-10-26
BR112014001110A2 (pt) 2017-02-14
RU2553262C1 (ru) 2015-06-10
EP2734488B1 (de) 2016-10-05
EP2734488A1 (de) 2014-05-28
US20140212957A1 (en) 2014-07-31
MX2014000655A (es) 2014-11-13
CN103781745A (zh) 2014-05-07
MY165921A (en) 2018-05-18
CA2841089A1 (en) 2013-01-24
BR112014001110A8 (pt) 2018-04-03
KR20140076548A (ko) 2014-06-20

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Legal Events

Date Code Title Description
FG Grant or registration
HC Change of company name or juridical status

Owner name: THYSSENKRUPP INDUSTRIAL SOLUTIONS AG

PD Change of proprietorship

Owner name: THYSSENKRUPP INDUSTRIAL SOLUTIONS AG