DD202142A5 - Verfahren zur herstellung von 3,3-dimethylglutarsaeure - Google Patents

Verfahren zur herstellung von 3,3-dimethylglutarsaeure Download PDF

Info

Publication number: DD202142A5
Authority: DD; German Democratic Republic
Prior art keywords: acid; stage; solution; ozone; oxo
Prior art date: 1981-05-12

Application number

DD82239718A

Other languages

German (de)

English (en)

Inventor

Pavel Lehky

Peter Hardt

Original Assignee

Lonza 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.)

1981-05-12

Filing date

1982-05-10

Publication date

1983-08-31

1982-05-10 Application filed by Lonza Ag filed Critical Lonza Ag

1983-08-31 Publication of DD202142A5 publication Critical patent/DD202142A5/de

Links

238000000034 method Methods 0.000 title claims abstract description 13
DUHQIGLHYXLKAE-UHFFFAOYSA-N 3,3-dimethylglutaric acid Chemical compound OC(=O)CC(C)(C)CC(O)=O DUHQIGLHYXLKAE-UHFFFAOYSA-N 0.000 title claims abstract description 11
238000002360 preparation method Methods 0.000 title claims description 6
HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 claims abstract description 32
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims abstract description 24
CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 claims abstract description 13
230000007062 hydrolysis Effects 0.000 claims abstract description 8
238000006460 hydrolysis reaction Methods 0.000 claims abstract description 8
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 23
239000002253 acid Substances 0.000 claims description 14
238000006243 chemical reaction Methods 0.000 claims description 7
239000002904 solvent Substances 0.000 claims description 6
238000005949 ozonolysis reaction Methods 0.000 claims description 5
238000009835 boiling Methods 0.000 claims description 4
150000007513 acids Chemical class 0.000 claims description 3
SLBXWQKHHZUDAY-UHFFFAOYSA-N 3,3-dimethyl-5-oxohexanoic acid Chemical compound CC(=O)CC(C)(C)CC(O)=O SLBXWQKHHZUDAY-UHFFFAOYSA-N 0.000 abstract description 8
239000000243 solution Substances 0.000 description 21
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 9
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
239000000047 product Substances 0.000 description 9
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 8
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
238000004817 gas chromatography Methods 0.000 description 6
BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 6
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
239000007864 aqueous solution Substances 0.000 description 4
239000007788 liquid Substances 0.000 description 4
239000000203 mixture Substances 0.000 description 4
OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
150000002148 esters Chemical class 0.000 description 3
235000019253 formic acid Nutrition 0.000 description 3
239000001301 oxygen Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
229920006395 saturated elastomer Polymers 0.000 description 3
239000000725 suspension Substances 0.000 description 3
BTUDGPVTCYNYLK-UHFFFAOYSA-N 2,2-dimethylglutaric acid Chemical compound OC(=O)C(C)(C)CCC(O)=O BTUDGPVTCYNYLK-UHFFFAOYSA-N 0.000 description 2
VUCHCMORNIRINY-UHFFFAOYSA-N 3,3-dimethyl-2-oxohexanoic acid Chemical compound CCCC(C)(C)C(=O)C(O)=O VUCHCMORNIRINY-UHFFFAOYSA-N 0.000 description 2
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 2
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
229910019142 PO4 Inorganic materials 0.000 description 2
WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
229910000147 aluminium phosphate Inorganic materials 0.000 description 2
230000015572 biosynthetic process Effects 0.000 description 2
238000001816 cooling Methods 0.000 description 2
238000001704 evaporation Methods 0.000 description 2
230000008020 evaporation Effects 0.000 description 2
239000012535 impurity Substances 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
238000006385 ozonation reaction Methods 0.000 description 2
150000002978 peroxides Chemical class 0.000 description 2
235000021317 phosphate Nutrition 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
150000003839 salts Chemical class 0.000 description 2
GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
239000007858 starting material Substances 0.000 description 2
238000003786 synthesis reaction Methods 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Natural products CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 1
WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
239000005708 Sodium hypochlorite Substances 0.000 description 1
238000009825 accumulation Methods 0.000 description 1
239000000654 additive Substances 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
150000001298 alcohols Chemical class 0.000 description 1
125000001931 aliphatic group Chemical group 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
239000002826 coolant Substances 0.000 description 1
239000012043 crude product Substances 0.000 description 1
239000013078 crystal Substances 0.000 description 1
230000006378 damage Effects 0.000 description 1
BADXJIPKFRBFOT-UHFFFAOYSA-N dimedone Chemical compound CC1(C)CC(=O)CC(=O)C1 BADXJIPKFRBFOT-UHFFFAOYSA-N 0.000 description 1
238000004821 distillation Methods 0.000 description 1
ZIUSEGSNTOUIPT-UHFFFAOYSA-N ethyl 2-cyanoacetate Chemical compound CCOC(=O)CC#N ZIUSEGSNTOUIPT-UHFFFAOYSA-N 0.000 description 1
239000012467 final product Substances 0.000 description 1
239000007789 gas Substances 0.000 description 1
150000008282 halocarbons Chemical class 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
238000002955 isolation Methods 0.000 description 1
239000010687 lubricating oil Substances 0.000 description 1
239000000463 material Substances 0.000 description 1
PVRJOEAYRBQPLF-UHFFFAOYSA-N n-(2-hydroxypropyl)-n-(2-oxopropyl)nitrous amide Chemical compound CC(O)CN(N=O)CC(C)=O PVRJOEAYRBQPLF-UHFFFAOYSA-N 0.000 description 1
FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
239000010452 phosphate Substances 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000012266 salt solution Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
239000011780 sodium chloride Substances 0.000 description 1
AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 1
SUKJFIGYRHOWBL-UHFFFAOYSA-N sodium hypochlorite Chemical compound [Na+].Cl[O-] SUKJFIGYRHOWBL-UHFFFAOYSA-N 0.000 description 1
235000010265 sodium sulphite Nutrition 0.000 description 1
238000003756 stirring Methods 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/16—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation
- C07C51/285—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with peroxy-compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C07C51/34—Preparation of carboxylic acids or their salts, halides or anhydrides by oxidation with ozone; by hydrolysis of ozonides

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

DD82239718A 1981-05-12 1982-05-10 Verfahren zur herstellung von 3,3-dimethylglutarsaeure DD202142A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH3061/81A CH649981A5 (de)	1981-05-12	1981-05-12	Verfahren zur herstellung von 3,3-dimethylglutarsaeure.

Publications (1)

Publication Number	Publication Date
DD202142A5 true DD202142A5 (de)	1983-08-31

Family

ID=4247742

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD82239718A DD202142A5 (de)	1981-05-12	1982-05-10	Verfahren zur herstellung von 3,3-dimethylglutarsaeure

Country Status (13)

Country	Link
US (1)	US4511734A (da)
EP (1)	EP0064634B1 (da)
JP (1)	JPS57192329A (da)
AT (1)	ATE8614T1 (da)
CA (1)	CA1184934A (da)
CH (1)	CH649981A5 (da)
DD (1)	DD202142A5 (da)
DE (1)	DE3260447D1 (da)
DK (1)	DK197882A (da)
HU (1)	HU190008B (da)
IE (1)	IE52914B1 (da)
IL (1)	IL65733A (da)
SU (1)	SU1138018A3 (da)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP3866968A4 (en) *	2018-10-19	2022-07-27	P2 Science, Inc.	NEW METHODS FOR THE DISPROPORTIONATION DETERRENCE OF OZONIDES

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2971915A (en) *	1957-02-11	1961-02-14	Shell Oil Co	Lubricating oil compositions
DE2303925C3 (de) *	1973-01-26	1980-09-11	Vsesojuznyj Nautschno-Issledovatelskij Institut Neftechimitscheskich Processov Ssr, Leningrad (Sowjetunion)	Verfahren zur Herstellung von aliphatischen Dicarbonsäuren
PT67818A (en) *	1977-03-28	1978-04-01	Union Carbide Corp	Process for the synthesis of biocidal 2-aryl-1,3-cycloalkanedionas and their enol esters
US4340753A (en) *	1980-09-02	1982-07-20	General Electric Company	Method for making keto acids and dione cyclics obtained therefrom

1981
- 1981-05-12 CH CH3061/81A patent/CH649981A5/de not_active IP Right Cessation
1982
- 1982-04-21 EP EP82103381A patent/EP0064634B1/de not_active Expired
- 1982-04-21 AT AT82103381T patent/ATE8614T1/de not_active IP Right Cessation
- 1982-04-21 DE DE8282103381T patent/DE3260447D1/de not_active Expired
- 1982-04-29 IE IE1006/82A patent/IE52914B1/en unknown
- 1982-05-03 DK DK197882A patent/DK197882A/da not_active Application Discontinuation
- 1982-05-05 US US06/375,343 patent/US4511734A/en not_active Expired - Fee Related
- 1982-05-10 DD DD82239718A patent/DD202142A5/de unknown
- 1982-05-10 HU HU821457A patent/HU190008B/hu unknown
- 1982-05-11 IL IL65733A patent/IL65733A/xx unknown
- 1982-05-11 SU SU3433129A patent/SU1138018A3/ru active
- 1982-05-11 JP JP57079085A patent/JPS57192329A/ja active Pending
- 1982-05-12 CA CA000402779A patent/CA1184934A/en not_active Expired

Also Published As

Publication number	Publication date
EP0064634B1 (de)	1984-07-25
DK197882A (da)	1982-11-13
IL65733A (en)	1986-01-31
CH649981A5 (de)	1985-06-28
JPS57192329A (en)	1982-11-26
IL65733A0 (en)	1982-08-31
EP0064634A1 (de)	1982-11-17
US4511734A (en)	1985-04-16
IE821006L (en)	1982-11-12
DE3260447D1 (en)	1984-08-30
SU1138018A3 (ru)	1985-01-30
IE52914B1 (en)	1988-04-13
ATE8614T1 (de)	1984-08-15
HU190008B (en)	1986-08-28
CA1184934A (en)	1985-04-02

Publication	Publication Date	Title
DE2834547A1 (de)	1979-02-22	Herstellung von (1r,cis)-caronaldehydsaeure
EP0048373B1 (de)	1984-05-09	Verfahren zur Herstellung von Pyrazol
EP0415214A2 (de)	1991-03-06	Verfahren zur Herstellung von alpha-Fluoracrylsäurederivaten
DE2404160C3 (de)	1981-05-21	Verfahren zur Herstellung von 2-(4-Alkylphenyl)-propionsäuren
EP0064634B1 (de)	1984-07-25	Verfahren zur Herstellung von 3,3-Dimethylglutarsäure
CH619206A5 (da)	1980-09-15
EP0065707B1 (de)	1985-04-17	Verfahren zur Herstellung von Dimedon
EP0176026A1 (de)	1986-04-02	Verfahren zur Herstellung von 2,4-Dichlor-5-fluor-benzoesäure
EP0533013A2 (de)	1993-03-24	Verfahren zur Herstellung von 1-Fluor-cyclopropan-1-carbonsäure
AT392782B (de)	1991-06-10	Verfahren zur herstellung von alpha-(p-tent.- butylphenyl)-4-(hydroxydiphenylmethyl)-1- piperidinobutanol
DE2365683A1 (de)	1975-11-27	Neue eburanderivate und deren stereoisomere sowie verfahren zu deren herstellung
EP0065706B1 (de)	1985-01-16	Verfahren zur Herstellung von 3,3-Dimethylglutarsäure oder deren Ester
EP0423595B1 (de)	1994-05-18	Verfahren zur Herstellung von 3-Trichlormethyl-pyridin
EP0064633B1 (de)	1984-09-12	Verfahren zur Herstellung von 3,3-Dimethylglutarsäure
DD213437A5 (de)	1984-09-12	Verfahren zur herstellung von cyclopentenderivaten
EP1401845A1 (de)	2004-03-31	Verfahren zur herstellung von n-phosphonomethylglycin
AT393503B (de)	1991-11-11	Verfahren zur herstellung von malonsaeurederivaten durch ozonolyse von ungesaettigten verbindungen
DE1518246C (de)	1972-05-31	Verfahren zur Herstellung von Saccharose estern von substituierten Stearinsäuren
EP0087097B1 (de)	1987-05-13	2-Alkyl-1,3-diacyloxy-4-hydroxy-1-butene, ihre Herstellung und Verwendung
EP0678515A1 (de)	1995-10-25	Verfahren und Zwischenprodukte zur Herstellung von 5-Oxaspiro 2.4 heptan-6-on
US4296251A (en)	1981-10-20	Synthesis of (+)-cis-homocaronic acid
EP1016654A2 (de)	2000-07-05	Verfahren zur Herstellung von substituierten aromatischen und heteroaromatischen Aldehyden und Carbonsäuren
CH654577A5 (de)	1986-02-28	Verfahren zur herstellung von 6-methylnikotinsaeureester.
DD202139A5 (de)	1983-08-31	Verfahren zur herstellung von dimedon
CH673456A5 (en)	1990-03-15	2-Acetyl nicotinic acid prodn. - by ozonising 8-methyl-quinoline in solvent mixt. of acetic and sulphuric acids and treating reaction mixt. with hydrogen peroxide