JP2000515176A - 置換カルボキシル化誘導体 - Google Patents

置換カルボキシル化誘導体

Info

Publication number: JP2000515176A
Authority: JP; Japan
Prior art keywords: acid; substituted; reaction; hydrocarbyl; temperature
Prior art date: 1996-06-10
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.): Pending

Application number

JP10501334A

Other languages

English (en)

Japanese (ja)

Inventor

ブラックボロー，ジョン，リチャード

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.)

BP Chemicals Ltd

Original Assignee

BP Chemicals Ltd

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.)

1996-06-10

Filing date

1997-05-28

Publication date

2000-11-14

1996-06-10 Priority claimed from GBGB9612138.9A external-priority patent/GB9612138D0/en

1996-08-22 Priority claimed from GBGB9617615.1A external-priority patent/GB9617615D0/en

1996-10-04 Priority claimed from GBGB9620761.8A external-priority patent/GB9620761D0/en

1997-05-28 Application filed by BP Chemicals Ltd filed Critical BP Chemicals Ltd

2000-11-14 Publication of JP2000515176A publication Critical patent/JP2000515176A/ja

Status Pending legal-status Critical Current

Links

238000006243 chemical reaction Methods 0.000 claims abstract description 57
238000000034 method Methods 0.000 claims abstract description 49
229920000098 polyolefin Polymers 0.000 claims abstract description 28
-1 carboxylic acid compound Chemical class 0.000 claims abstract description 27
229940014800 succinic anhydride Drugs 0.000 claims abstract description 12
FALRKNHUBBKYCC-UHFFFAOYSA-N 2-(chloromethyl)pyridine-3-carbonitrile Chemical class ClCC1=NC=CC=C1C#N FALRKNHUBBKYCC-UHFFFAOYSA-N 0.000 claims abstract description 10
239000000654 additive Substances 0.000 claims abstract description 8
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 claims abstract description 8
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 8
229920002554 vinyl polymer Polymers 0.000 claims abstract description 8
230000003197 catalytic effect Effects 0.000 claims abstract description 4
239000002253 acid Substances 0.000 claims description 35
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 17
239000011541 reaction mixture Substances 0.000 claims description 14
229920000768 polyamine Polymers 0.000 claims description 13
239000000376 reactant Substances 0.000 claims description 11
NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims description 8
125000004432 carbon atom Chemical group C* 0.000 claims description 8
230000015572 biosynthetic process Effects 0.000 claims description 7
150000002148 esters Chemical class 0.000 claims description 7
238000004519 manufacturing process Methods 0.000 claims description 6
150000001412 amines Chemical class 0.000 claims description 5
150000008064 anhydrides Chemical group 0.000 claims description 5
150000001875 compounds Chemical class 0.000 claims description 5
150000005673 monoalkenes Chemical class 0.000 claims description 5
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 claims description 4
150000007513 acids Chemical class 0.000 claims description 4
229910000147 aluminium phosphate Inorganic materials 0.000 claims description 4
125000003118 aryl group Chemical group 0.000 claims description 4
OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 3
125000000217 alkyl group Chemical group 0.000 claims description 3
229920001577 copolymer Polymers 0.000 claims description 3
229920001519 homopolymer Polymers 0.000 claims description 3
238000011065 in-situ storage Methods 0.000 claims description 3
229920001083 polybutene Polymers 0.000 claims description 3
150000003839 salts Chemical class 0.000 claims description 3
SASYHUDIOGGZCN-ARJAWSKDSA-N (z)-2-ethylbut-2-enedioic acid Chemical compound CC\C(C(O)=O)=C\C(O)=O SASYHUDIOGGZCN-ARJAWSKDSA-N 0.000 claims description 2
VILCJCGEZXAXTO-UHFFFAOYSA-N 2,2,2-tetramine Chemical compound NCCNCCNCCN VILCJCGEZXAXTO-UHFFFAOYSA-N 0.000 claims description 2
JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
AXGOOCLYBPQWNG-UHFFFAOYSA-N 3-ethylfuran-2,5-dione Chemical compound CCC1=CC(=O)OC1=O AXGOOCLYBPQWNG-UHFFFAOYSA-N 0.000 claims description 2
AYKYXWQEBUNJCN-UHFFFAOYSA-N 3-methylfuran-2,5-dione Chemical compound CC1=CC(=O)OC1=O AYKYXWQEBUNJCN-UHFFFAOYSA-N 0.000 claims description 2
OFNISBHGPNMTMS-UHFFFAOYSA-N 3-methylideneoxolane-2,5-dione Chemical compound C=C1CC(=O)OC1=O OFNISBHGPNMTMS-UHFFFAOYSA-N 0.000 claims description 2
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 claims description 2
239000004743 Polypropylene Substances 0.000 claims description 2
125000003545 alkoxy group Chemical group 0.000 claims description 2
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 2
VSCWAEJMTAWNJL-UHFFFAOYSA-K aluminium trichloride Chemical compound Cl[Al](Cl)Cl VSCWAEJMTAWNJL-UHFFFAOYSA-K 0.000 claims description 2
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 claims description 2
229940092714 benzenesulfonic acid Drugs 0.000 claims description 2
125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 2
HNEGQIOMVPPMNR-IHWYPQMZSA-N citraconic acid Chemical compound OC(=O)C(/C)=C\C(O)=O HNEGQIOMVPPMNR-IHWYPQMZSA-N 0.000 claims description 2
229940018557 citraconic acid Drugs 0.000 claims description 2
IUNMPGNGSSIWFP-UHFFFAOYSA-N dimethylaminopropylamine Chemical compound CN(C)CCCN IUNMPGNGSSIWFP-UHFFFAOYSA-N 0.000 claims description 2
150000003949 imides Chemical class 0.000 claims description 2
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
239000011976 maleic acid Substances 0.000 claims description 2
LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
125000004433 nitrogen atom Chemical group N* 0.000 claims description 2
229920000642 polymer Polymers 0.000 claims description 2
229920001155 polypropylene Polymers 0.000 claims description 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
150000003460 sulfonic acids Chemical class 0.000 claims description 2
FAGUFWYHJQFNRV-UHFFFAOYSA-N tetraethylenepentamine Chemical compound NCCNCCNCCNCCN FAGUFWYHJQFNRV-UHFFFAOYSA-N 0.000 claims description 2
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 2
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 claims description 2
150000001720 carbohydrates Chemical class 0.000 claims 2
229910052751 metal Inorganic materials 0.000 claims 2
239000002184 metal Substances 0.000 claims 2
WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims 1
LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims 1
QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims 1
ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims 1
239000005642 Oleic acid Substances 0.000 claims 1
150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
125000003916 ethylene diamine group Chemical group 0.000 claims 1
238000007306 functionalization reaction Methods 0.000 claims 1
125000001183 hydrocarbyl group Chemical group 0.000 claims 1
150000004679 hydroxides Chemical class 0.000 claims 1
QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims 1
ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims 1
230000035322 succinylation Effects 0.000 abstract description 7
238000010613 succinylation reaction Methods 0.000 abstract description 7
230000002378 acidificating effect Effects 0.000 abstract description 2
230000000630 rising effect Effects 0.000 abstract 1
239000000047 product Substances 0.000 description 16
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 10
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 8
229920005652 polyisobutylene succinic anhydride Polymers 0.000 description 8
239000011347 resin Substances 0.000 description 6
229920005989 resin Polymers 0.000 description 6
KZNICNPSHKQLFF-UHFFFAOYSA-N succinimide Chemical class O=C1CCC(=O)N1 KZNICNPSHKQLFF-UHFFFAOYSA-N 0.000 description 6
VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 4
IAQRGUVFOMOMEM-UHFFFAOYSA-N butene Natural products CC=CC IAQRGUVFOMOMEM-UHFFFAOYSA-N 0.000 description 4
230000000052 comparative effect Effects 0.000 description 4
238000002474 experimental method Methods 0.000 description 4
239000000446 fuel Substances 0.000 description 4
239000000203 mixture Substances 0.000 description 4
229910052757 nitrogen Inorganic materials 0.000 description 4
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 description 3
229920002367 Polyisobutene Polymers 0.000 description 3
239000003795 chemical substances by application Substances 0.000 description 3
239000012065 filter cake Substances 0.000 description 3
239000000314 lubricant Substances 0.000 description 3
239000002904 solvent Substances 0.000 description 3
229960002317 succinimide Drugs 0.000 description 3
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 3
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
229920002368 Glissopal ® Polymers 0.000 description 2
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
239000003054 catalyst Substances 0.000 description 2
239000000706 filtrate Substances 0.000 description 2
239000000295 fuel oil Substances 0.000 description 2
239000010687 lubricating oil Substances 0.000 description 2
239000000463 material Substances 0.000 description 2
150000007524 organic acids Chemical class 0.000 description 2
230000035484 reaction time Effects 0.000 description 2
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 description 2
SYIUWAVTBADRJG-UHFFFAOYSA-N 2H-pyran-2,6(3H)-dione Chemical compound O=C1CC=CC(=O)O1 SYIUWAVTBADRJG-UHFFFAOYSA-N 0.000 description 1
LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
150000001336 alkenes Chemical class 0.000 description 1
LHIJANUOQQMGNT-UHFFFAOYSA-N aminoethylethanolamine Chemical compound NCCNCCO LHIJANUOQQMGNT-UHFFFAOYSA-N 0.000 description 1
238000004458 analytical method Methods 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
239000012298 atmosphere Substances 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
238000004140 cleaning Methods 0.000 description 1
238000002485 combustion reaction Methods 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
150000001993 dienes Chemical class 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
238000009472 formulation Methods 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
239000012535 impurity Substances 0.000 description 1
239000003112 inhibitor Substances 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
230000001050 lubricating effect Effects 0.000 description 1
150000002736 metal compounds Chemical class 0.000 description 1
229910000000 metal hydroxide Inorganic materials 0.000 description 1
150000004692 metal hydroxides Chemical class 0.000 description 1
229910044991 metal oxide Inorganic materials 0.000 description 1
150000004706 metal oxides Chemical class 0.000 description 1
239000012299 nitrogen atmosphere Substances 0.000 description 1
239000003973 paint Substances 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
239000013049 sediment Substances 0.000 description 1
229920002545 silicone oil Polymers 0.000 description 1
239000000779 smoke Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
RINCXYDBBGOEEQ-UHFFFAOYSA-N succinic anhydride Chemical class O=C1CCC(=O)O1 RINCXYDBBGOEEQ-UHFFFAOYSA-N 0.000 description 1
125000002730 succinyl group Chemical group C(CCC(=O)*)(=O)* 0.000 description 1
238000007039 two-step reaction Methods 0.000 description 1
239000002699 waste material Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F8/00—Chemical modification by after-treatment
- C08F8/46—Reaction with unsaturated dicarboxylic acids or anhydrides thereof, e.g. maleinisation

Landscapes

Chemical & Material Sciences (AREA)
General Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

JP10501334A 1996-06-10 1997-05-28 置換カルボキシル化誘導体 Pending JP2000515176A (ja)

Applications Claiming Priority (7)

Application Number	Priority Date	Filing Date	Title
GB9612138.9		1996-06-10
GBGB9612138.9A GB9612138D0 (en)	1996-06-10	1996-06-10	Substituted carboxylated derivatives
GB9617615.1		1996-08-22
GBGB9617615.1A GB9617615D0 (en)	1996-08-22	1996-08-22	Substituted carboxylated derivatives
GBGB9620761.8A GB9620761D0 (en)	1996-10-04	1996-10-04	Substituted carboxylated derivatives
GB9620761.8		1996-10-04
PCT/GB1997/001447 WO1997047666A1 (en)	1996-06-10	1997-05-28	Substituted carboxylated derivatives

Publications (1)

Publication Number	Publication Date
JP2000515176A true JP2000515176A (ja)	2000-11-14

Family

ID=27268314

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
JP10501334A Pending JP2000515176A (ja)	1996-06-10	1997-05-28	置換カルボキシル化誘導体

Country Status (6)

Country	Link
EP (1)	EP0910590A1 (id)
JP (1)	JP2000515176A (id)
CN (1)	CN1221431A (id)
AU (1)	AU2968697A (id)
ID (1)	ID17124A (id)
WO (1)	WO1997047666A1 (id)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2000178315A (ja) *	1998-12-15	2000-06-27	Chevron Chem Co Llc	ポリアルキレンスクシンイミドおよびその後処理誘導体

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US6451920B1 (en) *	1999-11-09	2002-09-17	Chevron Chemical Company Llc	Process for making polyalkylene/maleic anhydride copolymer
ITMI20071445A1 (it) *	2007-07-18	2009-01-19	Eni Spa	Polialchenil succinimmidi e loro impiego come disperdenti in oli lubrificanti
ITMI20071446A1 (it) *	2007-07-18	2009-01-19	Eni Spa	Polialchenil siccinimmidi e loro impiego come detergenti per carburanti
US20100160193A1 (en) *	2008-12-22	2010-06-24	Chevron Oronite LLC	Additive composition and method of making the same
WO2016089507A1 (en) *	2014-12-04	2016-06-09	Exxonmobil Chemical Patents Inc.	Water-based polyolefin corrosion inhibitors based on vinyl/vinylidene terminated polyolefins

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0014288B1 (en) *	1978-12-07	1983-06-08	Exxon Research And Engineering Company	Process for producing oil soluble derivatives of unsaturated c4-c10 dicarboxylic acid materials
WO1982000466A1 (en) *	1980-08-06	1982-02-18	Cane C	Polyalkenyl bis(succinic anhydrides or acids)their preparation and use
GB8818711D0 (en) *	1988-08-05	1988-09-07	Shell Int Research	Lubricating oil dispersants
TW242630B (id) *	1991-11-15	1995-03-11	Shell Internat Res Schappej B V
GB9309121D0 (en) *	1993-05-04	1993-06-16	Bp Chem Int Ltd	Substituted acylating agents

1997
- 1997-05-28 CN CN 97195403 patent/CN1221431A/zh active Pending
- 1997-05-28 WO PCT/GB1997/001447 patent/WO1997047666A1/en not_active Ceased
- 1997-05-28 AU AU29686/97A patent/AU2968697A/en not_active Abandoned
- 1997-05-28 EP EP97924115A patent/EP0910590A1/en not_active Withdrawn
- 1997-05-28 JP JP10501334A patent/JP2000515176A/ja active Pending
- 1997-06-10 ID IDP971979A patent/ID17124A/id unknown

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP2000178315A (ja) *	1998-12-15	2000-06-27	Chevron Chem Co Llc	ポリアルキレンスクシンイミドおよびその後処理誘導体

Also Published As

Publication number	Publication date
AU2968697A (en)	1998-01-07
CN1221431A (zh)	1999-06-30
WO1997047666A1 (en)	1997-12-18
EP0910590A1 (en)	1999-04-28
ID17124A (id)	1997-12-04

Publication	Publication Date	Title
US3912764A (en)	1975-10-14	Preparation of alkenyl succinic anhydrides
EP2414432B1 (en)	2017-05-31	Amine-terminated telechelic polymers and precursors thereto and methods for their preparation
CN1088944A (zh)	1994-07-06	由乙烯和1-丁烯衍生的聚合物用于制备润滑剂分散添加剂
JP2001503464A (ja)	2001-03-13	ポリオレフィン及びその官能化した誘導体
JPH05230131A (ja)	1993-09-07	不飽和ジカルボン酸物質のポリアルケニル誘導体の製造方法
CA2471534C (en)	2009-09-22	Low sediment process for thermally reacting highly reactive polymers and enophiles
JP2000515176A (ja)	2000-11-14	置換カルボキシル化誘導体
GB2081274A (en)	1982-02-17	Polyalkenyl bis(succinic acids or anhydrides)
JP2001509825A (ja)	2001-07-24	置換ポリイソブテンの製造
KR20000016494A (ko)	2000-03-25	치환 카르복실화 유도체
JPH08283340A (ja)	1996-10-29	置換アシル化剤
EP0513157B1 (en)	1998-04-22	Fuel oil compositions and additives
JP2003507540A (ja)	2003-02-25	酸性基含有重合体を反応性求核基含有オーバーベース化組成物で縮合することににより得られる金属含有分散剤重合体
US5919275A (en)	1999-07-06	Fuel and lubricant additives, their preparation and fuel or lubricant compositions containing these additives
US4844827A (en)	1989-07-04	Lubricating oil additive
EP0738253B1 (en)	2001-09-05	Carbonyl containing compounds
EP0744393B1 (en)	2000-08-16	Process for the preparation of polyalkene-substituted succinic acylating agents in the presence of a dihelotriphenylphosphorane as catalysts
US6730747B1 (en)	2004-05-04	Carbonyl containing compounds
EP2176305B1 (en)	2019-09-04	Process to prepare polyalkenyl succinimides and use thereof as detergents for fuels
US6462140B2 (en)	2002-10-08	Carbonyl containing compounds
JPH08165480A (ja)	1996-06-25	燃料油用流動性向上剤
WO1982000466A1 (en)	1982-02-18	Polyalkenyl bis(succinic anhydrides or acids)their preparation and use
JPH01172409A (ja)	1989-07-07	多機能性６向上剤用の重合体アミド
JP2000505121A (ja)	2000-04-25	燃料及び潤滑剤添加剤

JP2000515176A - 置換カルボキシル化誘導体 - Google Patents

Info

Links

Classifications

Landscapes

Applications Claiming Priority (7)

Publications (1)

Family

ID=27268314

Family Applications (1)

Country Status (6)

Cited By (1)

Families Citing this family (5)

Family Cites Families (5)

Cited By (1)

Also Published As

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