JPS6210496B2 - - Google Patents

Info

Publication number: JPS6210496B2
Authority: JP; Japan
Prior art keywords: glutaraldehyde; cyclopentanediol; reaction; yield; cobalt
Prior art date: 1980-06-18
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.): Expired

Application number

JP8226580A

Other languages

English (en)

Japanese (ja)

Other versions

JPS577434A (en

Inventor

Yoshio Kamya

Atsuo Murata

Hiroo Kido

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.)

1980-06-18

Filing date

1980-06-18

Publication date

1987-03-06

1980-06-18 Application filed by Nissan Chemical Corp filed Critical Nissan Chemical Corp

1980-06-18 Priority to JP8226580A priority Critical patent/JPS577434A/ja

1982-01-14 Publication of JPS577434A publication Critical patent/JPS577434A/ja

1987-03-06 Publication of JPS6210496B2 publication Critical patent/JPS6210496B2/ja

Status Granted legal-status Critical Current

Links

SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims description 20
VCVOSERVUCJNPR-UHFFFAOYSA-N cyclopentane-1,2-diol Chemical compound OC1CCCC1O VCVOSERVUCJNPR-UHFFFAOYSA-N 0.000 claims description 13
150000001869 cobalt compounds Chemical class 0.000 claims description 6
QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 5
230000001590 oxidative effect Effects 0.000 claims description 5
239000001301 oxygen Substances 0.000 claims description 5
229910052760 oxygen Inorganic materials 0.000 claims description 5
238000004519 manufacturing process Methods 0.000 claims description 4
238000006243 chemical reaction Methods 0.000 description 9
239000003054 catalyst Substances 0.000 description 6
LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentene Chemical compound C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 6
238000007254 oxidation reaction Methods 0.000 description 6
238000000034 method Methods 0.000 description 5
MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 4
150000001732 carboxylic acid derivatives Chemical class 0.000 description 4
230000003647 oxidation Effects 0.000 description 4
JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 3
239000002994 raw material Substances 0.000 description 3
230000035484 reaction time Effects 0.000 description 3
238000003786 synthesis reaction Methods 0.000 description 3
HGINCPLSRVDWNT-UHFFFAOYSA-N Acrolein Chemical compound C=CC=O HGINCPLSRVDWNT-UHFFFAOYSA-N 0.000 description 2
KFSLWBXXFJQRDL-UHFFFAOYSA-N Peracetic acid Chemical compound CC(=O)OO KFSLWBXXFJQRDL-UHFFFAOYSA-N 0.000 description 2
150000001299 aldehydes Chemical class 0.000 description 2
-1 alkyl vinyl ether Chemical compound 0.000 description 2
239000007795 chemical reaction product Substances 0.000 description 2
239000000645 desinfectant Substances 0.000 description 2
GJEZBVHHZQAEDB-SYDPRGILSA-N (1s,5r)-6-oxabicyclo[3.1.0]hexane Chemical compound C1CC[C@H]2O[C@H]21 GJEZBVHHZQAEDB-SYDPRGILSA-N 0.000 description 1
OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
PNZVFASWDSMJER-UHFFFAOYSA-N acetic acid;lead Chemical compound [Pb].CC(O)=O PNZVFASWDSMJER-UHFFFAOYSA-N 0.000 description 1
125000003172 aldehyde group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
239000003153 chemical reaction reagent Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000001868 cobalt Chemical class 0.000 description 1
229910017052 cobalt Inorganic materials 0.000 description 1
239000010941 cobalt Substances 0.000 description 1
GVPFVAHMJGGAJG-UHFFFAOYSA-L cobalt dichloride Chemical compound [Cl-].[Cl-].[Co+2] GVPFVAHMJGGAJG-UHFFFAOYSA-L 0.000 description 1
CTIHZTFULZJBGQ-UHFFFAOYSA-L cobalt(2+);decanoate Chemical compound [Co+2].CCCCCCCCCC([O-])=O.CCCCCCCCCC([O-])=O CTIHZTFULZJBGQ-UHFFFAOYSA-L 0.000 description 1
FJDJVBXSSLDNJB-LNTINUHCSA-N cobalt;(z)-4-hydroxypent-3-en-2-one Chemical compound [Co].C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O.C\C(O)=C\C(C)=O FJDJVBXSSLDNJB-LNTINUHCSA-N 0.000 description 1
150000001875 compounds Chemical class 0.000 description 1
230000007423 decrease Effects 0.000 description 1
150000002009 diols Chemical group 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
239000010985 leather Substances 0.000 description 1
229910052748 manganese Inorganic materials 0.000 description 1
239000011572 manganese Substances 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
239000000203 mixture Substances 0.000 description 1
150000002762 monocarboxylic acid derivatives Chemical class 0.000 description 1
150000002816 nickel compounds Chemical class 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
238000007248 oxidative elimination reaction Methods 0.000 description 1
238000007086 side reaction Methods 0.000 description 1
239000002904 solvent Substances 0.000 description 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP8226580A 1980-06-18 1980-06-18 Preparation of glutaraldehyde Granted JPS577434A (en)

Priority Applications (1)

Application Number	Priority Date	Filing Date	Title
JP8226580A JPS577434A (en)	1980-06-18	1980-06-18	Preparation of glutaraldehyde

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
JP8226580A JPS577434A (en)	1980-06-18	1980-06-18	Preparation of glutaraldehyde

Publications (2)

Publication Number	Publication Date
JPS577434A JPS577434A (en)	1982-01-14
JPS6210496B2 true JPS6210496B2 (fr)	1987-03-06

Family

ID=13769637

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP8226580A Granted JPS577434A (en)	1980-06-18	1980-06-18	Preparation of glutaraldehyde

Country Status (1)

Country	Link
JP (1)	JPS577434A (fr)

1980
- 1980-06-18 JP JP8226580A patent/JPS577434A/ja active Granted

Also Published As

Publication number	Publication date
JPS577434A (en)	1982-01-14

Publication	Publication Date	Title
JP4955886B2 (ja)	2012-06-20	アルデヒドから脂肪族カルボン酸を製造する方法
JPS6361296B2 (fr)	1988-11-28
JPS6411010B2 (fr)	1989-02-23
NO142748B (no)	1980-06-30	Fremgangsmaate til fremstilling av metylakrylat eller en blanding av metylakrylat og akrylsyre
JP2006504781A (ja)	2006-02-09	カルボン酸の製造方法
JPS6210496B2 (fr)	1987-03-06
JPH07116097B2 (ja)	1995-12-13	ピロメリツト酸の製造方法
JPS5843936A (ja)	1983-03-14	グリコ−ルアルデヒドの製法
US4256650A (en)	1981-03-17	Process for preparing propylene oxide and acetic acid
US3637818A (en)	1972-01-25	Process for preparing mixtures of acetaldehyde acetic acid and vinyl acetate
EP1201637B1 (fr)	2005-03-16	Procédé pour la production d'acides carboxyliques insaturés
JP4692702B2 (ja)	2011-06-01	芳香族カルボン酸類の製造方法
JPS6153287A (ja)	1986-03-17	二環式アミドアセタールの製造方法
JP2548590B2 (ja)	1996-10-30	共役ジエンの選択的酸化カルボニル化方法
JPH021819B2 (fr)	1990-01-12
JPH02200653A (ja)	1990-08-08	１級アルコールからアルデヒドの製造法
JPH0427971B2 (fr)	1992-05-13
JPH0784397B2 (ja)	1995-09-13	（３−ビニルフエニル）フエニルメタン
KR100966141B1 (ko)	2010-06-25	카르복실산 에스테르 제조용 촉매 및 제조방법
JPH01117859A (ja)	1989-05-10	芳香族過カルボン酸の製造法
JPH0113704B2 (fr)	1989-03-07
KR101671429B1 (ko)	2016-11-01	벤조산의 제조 방법
JPS6081139A (ja)	1985-05-09	シクロペンタノンの製造方法
JPS5821642A (ja)	1983-02-08	アジピン酸の製造法
JPH06329567A (ja)	1994-11-29	１，６−ヘキサンジオールの製造方法