JPS5665843A - Isomerization of beta-gamma unsaturated ester - Google Patents

Isomerization of beta-gamma unsaturated ester

Info

Publication number: JPS5665843A
Authority: JP; Japan
Prior art keywords: unsaturated ester; isomerization; catalyst; disulfide; dithiol
Prior art date: 1979-11-02
Legal status (The legal status 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 status listed.): Granted

Application number

JP14242179A

Other languages

English (en)

Japanese (ja)

Other versions

JPS6225134B2 (cs

Inventor

Seiji Tsuchiya

Hideo Suzuki

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Nissan Chemical Corp

Original Assignee

Nissan Chemical Corp

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.)

1979-11-02

Filing date

1979-11-02

Publication date

1981-06-03

1979-11-02 Application filed by Nissan Chemical Corp filed Critical Nissan Chemical Corp

1979-11-02 Priority to JP14242179A priority Critical patent/JPS5665843A/ja

1980-05-23 Priority to US06/152,819 priority patent/US4338170A/en

1980-06-05 Priority to NL8003281A priority patent/NL8003281A/nl

1980-06-13 Priority to DE19803022296 priority patent/DE3022296A1/de

1980-06-13 Priority to GB8019391A priority patent/GB2054561B/en

1981-06-03 Publication of JPS5665843A publication Critical patent/JPS5665843A/ja

1987-06-01 Publication of JPS6225134B2 publication Critical patent/JPS6225134B2/ja

Status Granted legal-status Critical Current

Links

150000002148 esters Chemical class 0.000 title abstract 3
238000006317 isomerization reaction Methods 0.000 title abstract 2
239000003054 catalyst Substances 0.000 abstract 3
238000006243 chemical reaction Methods 0.000 abstract 3
RMVRSNDYEFQCLF-UHFFFAOYSA-N thiophenol Chemical compound SC1=CC=CC=C1 RMVRSNDYEFQCLF-UHFFFAOYSA-N 0.000 abstract 3
OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 abstract 2
GUUVPOWQJOLRAS-UHFFFAOYSA-N Diphenyl disulfide Chemical compound C=1C=CC=CC=1SSC1=CC=CC=C1 GUUVPOWQJOLRAS-UHFFFAOYSA-N 0.000 abstract 2
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract 2
239000011261 inert gas Substances 0.000 abstract 2
239000003999 initiator Substances 0.000 abstract 2
CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 abstract 2
AROCLDYPZXMJPW-UHFFFAOYSA-N 1-(octyldisulfanyl)octane Chemical compound CCCCCCCCSSCCCCCCCC AROCLDYPZXMJPW-UHFFFAOYSA-N 0.000 abstract 1
LXUNZSDDXMPKLP-UHFFFAOYSA-N 2-Methylbenzenethiol Chemical compound CC1=CC=CC=C1S LXUNZSDDXMPKLP-UHFFFAOYSA-N 0.000 abstract 1
PWOBDMNCYMQTCE-UHFFFAOYSA-N 2-chlorobenzenethiol Chemical compound SC1=CC=CC=C1Cl PWOBDMNCYMQTCE-UHFFFAOYSA-N 0.000 abstract 1
YNWSTXBQNLCEPJ-UHFFFAOYSA-N 3-decyl-3h-dithiole Chemical compound CCCCCCCCCCC1SSC=C1 YNWSTXBQNLCEPJ-UHFFFAOYSA-N 0.000 abstract 1
WRXOZRLZDJAYDR-UHFFFAOYSA-N 3-methylbenzenethiol Chemical compound CC1=CC=CC(S)=C1 WRXOZRLZDJAYDR-UHFFFAOYSA-N 0.000 abstract 1
WLHCBQAPPJAULW-UHFFFAOYSA-N 4-methylbenzenethiol Chemical compound CC1=CC=C(S)C=C1 WLHCBQAPPJAULW-UHFFFAOYSA-N 0.000 abstract 1
239000004215 Carbon black (E152) Substances 0.000 abstract 1
WVDYBOADDMMFIY-UHFFFAOYSA-N Cyclopentanethiol Chemical compound SC1CCCC1 WVDYBOADDMMFIY-UHFFFAOYSA-N 0.000 abstract 1
BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 abstract 1
HIGQPQRQIQDZMP-DHZHZOJOSA-N Neryl acetate Natural products CC(C)=CCC\C(C)=C\COC(C)=O HIGQPQRQIQDZMP-DHZHZOJOSA-N 0.000 abstract 1
ZVQOOHYFBIDMTQ-UHFFFAOYSA-N [methyl(oxido){1-[6-(trifluoromethyl)pyridin-3-yl]ethyl}-lambda(6)-sulfanylidene]cyanamide Chemical compound N#CN=S(C)(=O)C(C)C1=CC=C(C(F)(F)F)N=C1 ZVQOOHYFBIDMTQ-UHFFFAOYSA-N 0.000 abstract 1
125000000217 alkyl group Chemical group 0.000 abstract 1
CMKBCTPCXZNQKX-UHFFFAOYSA-N cyclohexanethiol Chemical compound SC1CCCCC1 CMKBCTPCXZNQKX-UHFFFAOYSA-N 0.000 abstract 1
150000004662 dithiols Chemical class 0.000 abstract 1
DNJIEGIFACGWOD-UHFFFAOYSA-N ethyl mercaptane Natural products CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 abstract 1
HIGQPQRQIQDZMP-UHFFFAOYSA-N geranil acetate Natural products CC(C)=CCCC(C)=CCOC(C)=O HIGQPQRQIQDZMP-UHFFFAOYSA-N 0.000 abstract 1
229930195733 hydrocarbon Natural products 0.000 abstract 1
150000002430 hydrocarbons Chemical class 0.000 abstract 1
HIGQPQRQIQDZMP-FLIBITNWSA-N neryl acetate Chemical compound CC(C)=CCC\C(C)=C/COC(C)=O HIGQPQRQIQDZMP-FLIBITNWSA-N 0.000 abstract 1
KZCOBXFFBQJQHH-UHFFFAOYSA-N octane-1-thiol Chemical compound CCCCCCCCS KZCOBXFFBQJQHH-UHFFFAOYSA-N 0.000 abstract 1
DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 0.000 abstract 1

Classifications

- Y—GENERAL 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

JP14242179A 1979-06-14 1979-11-02 Isomerization of beta-gamma unsaturated ester Granted JPS5665843A (en)

Priority Applications (5)

Application Number	Priority Date	Filing Date	Title
JP14242179A JPS5665843A (en)	1979-11-02	1979-11-02	Isomerization of beta-gamma unsaturated ester
US06/152,819 US4338170A (en)	1979-06-14	1980-05-23	Isomerization of β-γ-unsaturated alcohol or its ester
NL8003281A NL8003281A (nl)	1979-06-14	1980-06-05	Werkwijze voor het uitvoeren van een isomerisatie van een onverzadigde alkohol of een ester hiervan.
DE19803022296 DE3022296A1 (de)	1979-06-14	1980-06-13	Isomerisation von beta , gamma -ungesaettigtem alkohol oder dessen ester
GB8019391A GB2054561B (en)	1979-06-14	1980-06-13	Isomerization of y-unsaturated alcohol or its ester

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP14242179A JPS5665843A (en)	1979-11-02	1979-11-02	Isomerization of beta-gamma unsaturated ester

Publications (2)

Publication Number	Publication Date
JPS5665843A true JPS5665843A (en)	1981-06-03
JPS6225134B2 JPS6225134B2 (cs)	1987-06-01

Family

ID=15314931

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP14242179A Granted JPS5665843A (en)	1979-06-14	1979-11-02	Isomerization of beta-gamma unsaturated ester

Country Status (1)

Country	Link
JP (1)	JPS5665843A (cs)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2016506396A (ja) *	2012-12-18	2016-03-03	ディーエスエムアイピーアセッツビー．ブイ．	不飽和化合物のためのシス／トランス異性化触媒としてのポリチオール

1979
- 1979-11-02 JP JP14242179A patent/JPS5665843A/ja active Granted

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2016506396A (ja) *	2012-12-18	2016-03-03	ディーエスエムアイピーアセッツビー．ブイ．	不飽和化合物のためのシス／トランス異性化触媒としてのポリチオール

Also Published As

Publication number	Publication date
JPS6225134B2 (cs)	1987-06-01

Similar Documents

Publication	Publication Date	Title
JPS5575743A (en)	1980-06-07	Reactivation method for antimony-containing oxide catalyst
AU586515B2 (en)	1989-07-13	Mixtures crosslinkable by photopolymerization
JPS5665843A (en)	1981-06-03	Isomerization of beta-gamma unsaturated ester
IT8141664A0 (it)	1981-10-14	H 2 so 4 in presenza di so 2 in un procedimento per controllare so 3, ambiente di gas controllato contenente h 2 o.
AU544962B2 (en)	1985-06-27	Synthesis of prostaglandin analogues
GB1528724A (en)	1978-10-18	Process for refining gases
JPS5665832A (en)	1981-06-03	Isomerization of beta-gamma unsaturated alcohol
ES8206559A1 (es)	1982-08-16	Procedimiento para preparar un polimero de cloruro de vinilo
JPS51143583A (en)	1976-12-09	Method for regulating gas-phase chemical reaction
JPS5318933A (en)	1978-02-21	Execution method of interruptable order
FI862316A0 (fi)	1986-05-30	Vinylesterharts som frigoer en liten del styren i vilken anvaendes torkande oljor vid fiberfoerstaerkningstillaempning.
JPS5551421A (en)	1980-04-15	Deodorization
JPS5683434A (en)	1981-07-08	Preparation of aldehyde
JPS52105994A (en)	1977-09-06	Method for crossslinking or chainnextending hydrocarbon having ethylenic unsaturated groups
JPS57108103A (en)	1982-07-06	Oligomer composition
GB1314102A (en)	1973-04-18	Preparation of pesticidal s-vinylic esters of thiophosphorus acids by addition of phosphoryl disulphides to acetylenes
KR920000798A (ko)	1992-01-29	촉 매
KR840000235A (ko)	1984-02-18	치환 히드록시벤젠류에 의한 2-레노일메르캅토프로피온일글리신의 에스테르 제조방법 및 이를 함유한 약제조성물
JPS5226361A (en)	1977-02-26	Process for refining of harmful gases
JPS51113807A (en)	1976-10-07	Process for preparation of methacrolein and methacrylic acid and or 1, 3-butadiene
ATE70731T1 (de)	1992-01-15	Verfahren zum beseitigen von schwefeldioxid aus gasen.
JPS5239606A (en)	1977-03-28	Process for dehydrogensulfide of acetylene containing hydrogen sulfide
JPS55167236A (en)	1980-12-26	Isomerization of beta-alpha unsaturated alcohol
JPS52149759A (en)	1977-12-13	Chain containing device for hoist
JPS5724313A (en)	1982-02-08	Cis-trans isomerizing method of unsaturated compound