CH642937A5 - Verfahren zur herstellung bifunktioneller aliphatischer organischer verbindungen. - Google Patents

Verfahren zur herstellung bifunktioneller aliphatischer organischer verbindungen. Download PDF

Info

Publication number: CH642937A5
Authority: CH; Switzerland
Prior art keywords: acid; salt; bivalent; yield; cyclohexanone
Prior art date: 1978-06-26

Application number

CH595879A

Other languages

German (de)

English (en)

Inventor

Paolo Maggioni

Francesco Minisci

Attilio Citterio

Original Assignee

Brichima Spa

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.)

1978-06-26

Filing date

1979-06-26

Publication date

1984-05-15

1979-06-26 Application filed by Brichima Spa filed Critical Brichima Spa

1984-05-15 Publication of CH642937A5 publication Critical patent/CH642937A5/de

Links

230000001588 bifunctional effect Effects 0.000 title claims description 10
238000004519 manufacturing process Methods 0.000 title description 3
150000002894 organic compounds Chemical class 0.000 title 1
238000000034 method Methods 0.000 claims description 30
-1 aliphatic organic compounds Chemical class 0.000 claims description 15
150000003839 salts Chemical class 0.000 claims description 15
239000000203 mixture Substances 0.000 claims description 14
229910052751 metal Inorganic materials 0.000 claims description 11
239000002184 metal Substances 0.000 claims description 11
230000003197 catalytic effect Effects 0.000 claims description 9
125000004432 carbon atom Chemical group C* 0.000 claims description 8
230000009467 reduction Effects 0.000 claims description 8
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 7
239000002253 acid Substances 0.000 claims description 7
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
150000002739 metals Chemical class 0.000 claims description 5
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 5
150000001336 alkenes Chemical class 0.000 claims description 4
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
229910052739 hydrogen Inorganic materials 0.000 claims description 3
239000001257 hydrogen Substances 0.000 claims description 3
238000002360 preparation method Methods 0.000 claims description 3
125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 claims description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 claims description 2
239000003960 organic solvent Substances 0.000 claims description 2
LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 claims description 2
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical group O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 45
239000000047 product Substances 0.000 description 32
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 27
FRJDUBNRWRIHSI-UHFFFAOYSA-N 8-cyanooctanoic acid Chemical compound OC(=O)CCCCCCCC#N FRJDUBNRWRIHSI-UHFFFAOYSA-N 0.000 description 13
239000007864 aqueous solution Substances 0.000 description 13
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 12
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 12
238000006243 chemical reaction Methods 0.000 description 12
238000003756 stirring Methods 0.000 description 11
150000001875 compounds Chemical class 0.000 description 10
ISIQQQYKUPBYSL-UHFFFAOYSA-N undecanedinitrile Chemical compound N#CCCCCCCCCCC#N ISIQQQYKUPBYSL-UHFFFAOYSA-N 0.000 description 10
WWZKQHOCKIZLMA-UHFFFAOYSA-N Caprylic acid Natural products CCCCCCCC(O)=O WWZKQHOCKIZLMA-UHFFFAOYSA-N 0.000 description 8
GONOPSZTUGRENK-UHFFFAOYSA-N benzyl(trichloro)silane Chemical compound Cl[Si](Cl)(Cl)CC1=CC=CC=C1 GONOPSZTUGRENK-UHFFFAOYSA-N 0.000 description 8
FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 8
239000000243 solution Substances 0.000 description 8
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 6
230000015572 biosynthetic process Effects 0.000 description 6
125000000524 functional group Chemical group 0.000 description 5
150000002576 ketones Chemical class 0.000 description 5
230000007935 neutral effect Effects 0.000 description 5
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
229910021556 Chromium(III) chloride Inorganic materials 0.000 description 3
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 3
150000007824 aliphatic compounds Chemical class 0.000 description 3
229910052804 chromium Inorganic materials 0.000 description 3
QSWDMMVNRMROPK-UHFFFAOYSA-K chromium(3+) trichloride Chemical compound [Cl-].[Cl-].[Cl-].[Cr+3] QSWDMMVNRMROPK-UHFFFAOYSA-K 0.000 description 3
239000011636 chromium(III) chloride Substances 0.000 description 3
235000007831 chromium(III) chloride Nutrition 0.000 description 3
238000004821 distillation Methods 0.000 description 3
150000002432 hydroperoxides Chemical class 0.000 description 3
239000011541 reaction mixture Substances 0.000 description 3
229910052719 titanium Inorganic materials 0.000 description 3
DXNCZXXFRKPEPY-UHFFFAOYSA-N tridecanedioic acid Chemical compound OC(=O)CCCCCCCCCCCC(O)=O DXNCZXXFRKPEPY-UHFFFAOYSA-N 0.000 description 3
LWBHHRRTOZQPDM-UHFFFAOYSA-N undecanedioic acid Chemical compound OC(=O)CCCCCCCCCC(O)=O LWBHHRRTOZQPDM-UHFFFAOYSA-N 0.000 description 3
229910052720 vanadium Inorganic materials 0.000 description 3
239000004711 α-olefin Substances 0.000 description 3
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
229910052782 aluminium Inorganic materials 0.000 description 2
FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
239000006227 byproduct Substances 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
OCDXZFSOHJRGIL-UHFFFAOYSA-N cyclohexyloxycyclohexane Chemical compound C1CCCCC1OC1CCCCC1 OCDXZFSOHJRGIL-UHFFFAOYSA-N 0.000 description 2
NUKZAGXMHTUAFE-UHFFFAOYSA-N methyl hexanoate Chemical compound CCCCCC(=O)OC NUKZAGXMHTUAFE-UHFFFAOYSA-N 0.000 description 2
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 2
230000003647 oxidation Effects 0.000 description 2
238000007254 oxidation reaction Methods 0.000 description 2
239000004033 plastic Substances 0.000 description 2
229920003023 plastic Polymers 0.000 description 2
102200073741 rs121909602 Human genes 0.000 description 2
229910000029 sodium carbonate Inorganic materials 0.000 description 2
229920002994 synthetic fiber Polymers 0.000 description 2
239000012209 synthetic fiber Substances 0.000 description 2
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 1
BYFKKNYEIXWOQO-UHFFFAOYSA-N 9-oxo capric acid Chemical compound CC(=O)CCCCCCCC(O)=O BYFKKNYEIXWOQO-UHFFFAOYSA-N 0.000 description 1
HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
239000004952 Polyamide Substances 0.000 description 1
229910010062 TiCl3 Inorganic materials 0.000 description 1
239000000061 acid fraction Substances 0.000 description 1
230000004913 activation Effects 0.000 description 1
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
238000006701 autoxidation reaction Methods 0.000 description 1
150000001805 chlorine compounds Chemical class 0.000 description 1
GCFAUZGWPDYAJN-UHFFFAOYSA-N cyclohexyl 3-phenylprop-2-enoate Chemical compound C=1C=CC=CC=1C=CC(=O)OC1CCCCC1 GCFAUZGWPDYAJN-UHFFFAOYSA-N 0.000 description 1
DTNOERNOMHQUCN-UHFFFAOYSA-N cyclohexyl hexanoate Chemical compound CCCCCC(=O)OC1CCCCC1 DTNOERNOMHQUCN-UHFFFAOYSA-N 0.000 description 1
230000002950 deficient Effects 0.000 description 1
239000000539 dimer Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
230000032050 esterification Effects 0.000 description 1
238000005886 esterification reaction Methods 0.000 description 1
238000006266 etherification reaction Methods 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
230000007062 hydrolysis Effects 0.000 description 1
238000006460 hydrolysis reaction Methods 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
239000010687 lubricating oil Substances 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
OJURWUUOVGOHJZ-UHFFFAOYSA-N methyl 2-[(2-acetyloxyphenyl)methyl-[2-[(2-acetyloxyphenyl)methyl-(2-methoxy-2-oxoethyl)amino]ethyl]amino]acetate Chemical compound C=1C=CC=C(OC(C)=O)C=1CN(CC(=O)OC)CCN(CC(=O)OC)CC1=CC=CC=C1OC(C)=O OJURWUUOVGOHJZ-UHFFFAOYSA-N 0.000 description 1
150000004702 methyl esters Chemical class 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
239000004014 plasticizer Substances 0.000 description 1
229920002647 polyamide Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
239000000843 powder Substances 0.000 description 1
239000002994 raw material Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
238000006722 reduction reaction Methods 0.000 description 1
238000007142 ring opening reaction Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000000126 substance Substances 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
YONPGGFAJWQGJC-UHFFFAOYSA-K titanium(iii) chloride Chemical compound Cl[Ti](Cl)Cl YONPGGFAJWQGJC-UHFFFAOYSA-K 0.000 description 1
VMQYWGMQGRSDBH-UHFFFAOYSA-N tridecane-2,12-dione Chemical compound CC(=O)CCCCCCCCCC(C)=O VMQYWGMQGRSDBH-UHFFFAOYSA-N 0.000 description 1
239000013638 trimer Substances 0.000 description 1
229920002554 vinyl polymer Polymers 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc 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
- C07C51/347—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
- C07C51/373—Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by introduction of functional groups containing oxygen only in doubly bound form
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/61—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups
- C07C45/67—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton
- C07C45/68—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms
- C07C45/72—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reactions not involving the formation of >C = O groups by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms by reaction of compounds containing >C = O groups with the same or other compounds containing >C = O groups
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C49/00—Ketones; Ketenes; Dimeric ketenes; Ketonic chelates
- C07C49/04—Saturated compounds containing keto groups bound to acyclic carbon atoms
- C07C49/12—Ketones containing more than one keto group
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C51/00—Preparation of carboxylic acids or their salts, halides or anhydrides
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C67/00—Preparation of carboxylic acid esters
- C07C67/39—Preparation of carboxylic acid esters by oxidation of groups which are precursors for the acid moiety of the ester

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Chemical Kinetics & Catalysis (AREA)
Engineering & Computer Science (AREA)
Oil, Petroleum & Natural Gas (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

CH595879A 1978-06-26 1979-06-26 Verfahren zur herstellung bifunktioneller aliphatischer organischer verbindungen. CH642937A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
IT24949/78A IT1097281B (it)	1978-06-26	1978-06-26	Processo per la produzione di composti organici alifatici difunzionali

Publications (1)

Publication Number	Publication Date
CH642937A5 true CH642937A5 (de)	1984-05-15

Family

ID=11215235

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
CH595879A CH642937A5 (de)	1978-06-26	1979-06-26	Verfahren zur herstellung bifunktioneller aliphatischer organischer verbindungen.

Country Status (9)

Country	Link
JP (1)	JPS557277A (it)
BE (1)	BE877290A (it)
CA (1)	CA1150733A (it)
CH (1)	CH642937A5 (it)
DE (1)	DE2925518A1 (it)
FR (1)	FR2429768A1 (it)
GB (1)	GB2024216B (it)
IT (1)	IT1097281B (it)
NL (1)	NL7904981A (it)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3229300A1 (de) *	1982-08-05	1984-02-09	Haarmann & Reimer Gmbh, 3450 Holzminden	Aliphatische dicarbonsaeureester als riechstoffe und diese enthaltende parfuemkompositionen und parfuemierte produkte

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US2671810A (en) *	1952-05-24	1954-03-09	Du Pont	Long-chain diketones
DE1254141B (de) *	1959-12-31	1967-11-16	Montedison Spa	Verfahren zur Herstellung von alpha-Chlor- oder alpha-Bromderivaten gesaettigter aliphatischer Mono- oder Dicarbonsaeuren
NL141864B (nl) *	1971-05-01	1974-04-16	Stamicarbon	Werkwijze voor de bereiding van cyanoalkaancarbonzuren.

1978
- 1978-06-26 IT IT24949/78A patent/IT1097281B/it active
1979
- 1979-06-20 GB GB7921538A patent/GB2024216B/en not_active Expired
- 1979-06-21 FR FR7915890A patent/FR2429768A1/fr active Granted
- 1979-06-25 DE DE19792925518 patent/DE2925518A1/de not_active Withdrawn
- 1979-06-25 JP JP7922879A patent/JPS557277A/ja active Pending
- 1979-06-26 CH CH595879A patent/CH642937A5/de not_active IP Right Cessation
- 1979-06-26 NL NL7904981A patent/NL7904981A/xx not_active Application Discontinuation
- 1979-06-26 BE BE0/195978A patent/BE877290A/xx not_active IP Right Cessation
- 1979-06-26 CA CA000330594A patent/CA1150733A/en not_active Expired

Also Published As

Publication number	Publication date
NL7904981A (nl)	1979-12-28
CA1150733A (en)	1983-07-26
JPS557277A (en)	1980-01-19
IT1097281B (it)	1985-08-31
FR2429768A1 (fr)	1980-01-25
IT7824949A0 (it)	1978-06-26
GB2024216B (en)	1982-11-10
BE877290A (fr)	1979-10-15
DE2925518A1 (de)	1980-01-17
FR2429768B1 (it)	1982-12-31
GB2024216A (en)	1980-01-09

Legal Events

Date	Code	Title	Description
1986-02-28	PL	Patent ceased
2024-10-31	PL	Patent ceased

Publication	Publication Date	Title
DD146943A5 (de)	1981-03-11	Verfahren zur herstellung von acetaldehyd
DE4229914A1 (de)	1994-03-10	Verbessertes Verfahren zur Herstellung von R/S-Ï-Liponsäure oder R/S-â-Liponsäure
DE3124889A1 (de)	1982-08-19	Verfahren zur herstellung von sulfobetainen
DE2318941A1 (de)	1973-10-25	Verfahren zur herstellung von verbindungen mit polyfluoralkylgruppen
DE3133583A1 (de)	1982-07-08	Verfahren zur herstellung von hydroxyphenyl-aliphatischen saeurederivaten und katalysator dafuer
CH642937A5 (de)	1984-05-15	Verfahren zur herstellung bifunktioneller aliphatischer organischer verbindungen.
DE3123878A1 (de)	1982-04-15	Neue sulfobetaine und verfahren zu ihrer herstellung
DE2104020B2 (de)	1975-01-30	Verfahren zur Herstellung von Salzen von Sulfoalkylacrylat oder -methacrylat
DE2417615A1 (de)	1974-11-07	Cyclische ketone und verfahren zu ihrer herstellung
DE69623717T2 (de)	2003-05-15	Verfahren zur Herstellung von Alkylimidazolidinon(meth)acrylaten
DE2508452A1 (de)	1975-09-11	Verfahren zur herstellung von alkylphenolen
DE2436788A1 (de)	1976-02-12	Verfahren zur herstellung von alpha, beta-ungesaettigten carbonsaeureestern
DE2831555C2 (it)	1987-09-10
DD236521A1 (de)	1986-06-11	Verfahren zur herstellung von neuen 3,3,4-trimethyl-4-sulfomethyl-pyrrolidiniumbetainen
US4217290A (en)	1980-08-12	Process for preparing bifunctional aliphatic organic compounds
DE2548625A1 (de)	1976-05-06	Verfahren zur addition von mindestens drei chloratome enthaltendem methan an einen aethylenisch-ungesaettigten kohlenwasserstoff
CH644093A5 (de)	1984-07-13	Verfahren zur herstellung von 2,2-dihalogenvinyl-substituierten cyclopropancarbonsaeure-estern.
DE3517158A1 (de)	1985-11-21	Methyl-2-(2-hydroperoxy-2-propyl)-naphthalin-6- carboxylat und verfahren zu dessen herstellung
DE2649711A1 (de)	1977-05-05	Ungesaettigte carbonsaeuren und verfahren zu deren herstellung
DE1518625A1 (de)	1969-02-20	Verfahren zur Herstellung von Transadditionsprodukten von Olefinen
DE2521610C2 (de)	1981-01-15	Verfahren zur Herstellung von Arylessigsäuren und deren Estern
DE835140C (de)	1952-03-27	Verfahren zur Herstellung organischer Persaeureester aus Hydroperoxyden
DE3006745C2 (de)	1986-09-11	Verfahren zur Herstellung von normal langkettigen Alkancarbonsäuren mit 26 bis 36 Kohlenstoffatomen
DE2032809A1 (de)	1971-01-21	Verfahren zur Herstellung von 3 Hydroxyisoxazoldenvaten
DE1720519C3 (de)	1977-06-08	Verfahren zur Herstellung von Polyestern