GB1479902A - Esters and amides of trisubstituted hydroxyphenylalkanoic acids - Google Patents
Esters and amides of trisubstituted hydroxyphenylalkanoic acidsInfo
- Publication number
- GB1479902A GB1479902A GB41450/74A GB4145074A GB1479902A GB 1479902 A GB1479902 A GB 1479902A GB 41450/74 A GB41450/74 A GB 41450/74A GB 4145074 A GB4145074 A GB 4145074A GB 1479902 A GB1479902 A GB 1479902A
- Authority
- GB
- United Kingdom
- Prior art keywords
- group
- amides
- esters
- alkyl
- formula
- Prior art date
- 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
Links
- 150000001408 amides Chemical class 0.000 title abstract 6
- 150000002148 esters Chemical class 0.000 title abstract 6
- 239000002253 acid Substances 0.000 title abstract 3
- 150000007513 acids Chemical class 0.000 title abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 4
- 125000004429 atom Chemical group 0.000 abstract 4
- 125000006704 (C5-C6) cycloalkyl group Chemical group 0.000 abstract 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 abstract 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 238000006243 chemical reaction Methods 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- QWBBPBRQALCEIZ-UHFFFAOYSA-N 2,3-dimethylphenol Chemical compound CC1=CC=CC(O)=C1C QWBBPBRQALCEIZ-UHFFFAOYSA-N 0.000 abstract 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 abstract 2
- 150000001298 alcohols Chemical class 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 229920005862 polyol Polymers 0.000 abstract 2
- 150000003077 polyols Chemical class 0.000 abstract 2
- 125000006702 (C1-C18) alkyl group Chemical group 0.000 abstract 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- HPYRKUGDNKIOON-UHFFFAOYSA-N 2,3-dimethyl-6-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound CC1=CC=C(C(C)(C)CC(C)(C)C)C(O)=C1C HPYRKUGDNKIOON-UHFFFAOYSA-N 0.000 abstract 1
- FXNDIJDIPNCZQJ-UHFFFAOYSA-N 2,4,4-trimethylpent-1-ene Chemical compound CC(=C)CC(C)(C)C FXNDIJDIPNCZQJ-UHFFFAOYSA-N 0.000 abstract 1
- CKNFOPRJVDPXDD-UHFFFAOYSA-N 2-(5-tert-butyl-4-hydroxy-2,3-dimethylphenyl)acetonitrile Chemical compound CC1=C(C)C(CC#N)=CC(C(C)(C)C)=C1O CKNFOPRJVDPXDD-UHFFFAOYSA-N 0.000 abstract 1
- XQXPVVBIMDBYFF-UHFFFAOYSA-N 4-hydroxyphenylacetic acid Chemical class OC(=O)CC1=CC=C(O)C=C1 XQXPVVBIMDBYFF-UHFFFAOYSA-N 0.000 abstract 1
- ONTQNSMWUGQQOX-UHFFFAOYSA-N 6-tert-butyl-4-[(dimethylamino)methyl]-2,3-dimethylphenol Chemical compound CN(C)CC1=CC(C(C)(C)C)=C(O)C(C)=C1C ONTQNSMWUGQQOX-UHFFFAOYSA-N 0.000 abstract 1
- 239000004215 Carbon black (E152) Substances 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 abstract 1
- VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 abstract 1
- 230000029936 alkylation Effects 0.000 abstract 1
- 238000005804 alkylation reaction Methods 0.000 abstract 1
- 150000007962 benzene acetonitriles Chemical class 0.000 abstract 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- KXZJHVJKXJLBKO-UHFFFAOYSA-N chembl1408157 Chemical compound N=1C2=CC=CC=C2C(C(=O)O)=CC=1C1=CC=C(O)C=C1 KXZJHVJKXJLBKO-UHFFFAOYSA-N 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000002993 cycloalkylene group Chemical group 0.000 abstract 1
- 230000006866 deterioration Effects 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 229930195733 hydrocarbon Natural products 0.000 abstract 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 abstract 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- QOHGMEYPUKSMST-UHFFFAOYSA-N methyl 2-(4-hydroxyphenyl)propanoate Chemical class COC(=O)C(C)C1=CC=C(O)C=C1 QOHGMEYPUKSMST-UHFFFAOYSA-N 0.000 abstract 1
- 150000004702 methyl esters Chemical class 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 239000011368 organic material Substances 0.000 abstract 1
- KJIFKLIQANRMOU-UHFFFAOYSA-N oxidanium;4-methylbenzenesulfonate Chemical compound O.CC1=CC=C(S(O)(=O)=O)C=C1 KJIFKLIQANRMOU-UHFFFAOYSA-N 0.000 abstract 1
- 230000001590 oxidative effect Effects 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 230000000087 stabilizing effect Effects 0.000 abstract 1
- 125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 abstract 1
- 238000005809 transesterification reaction Methods 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
- C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
- C10M2219/085—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms containing carboxyl groups; Derivatives thereof
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
- C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
- C10M2221/04—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C10M2221/043—Polyoxyalkylene ethers with a thioether group
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
- C10N2040/00—Specified use or application for which the lubricating composition is intended
- C10N2040/20—Metal working
- C10N2040/22—Metal working with essential removal of material, e.g. cutting, grinding or drilling
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Fats And Perfumes (AREA)
- Lubricants (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Coating Of Shaped Articles Made Of Macromolecular Substances (AREA)
- Anti-Oxidant Or Stabilizer Compositions (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US40074573A | 1973-09-25 | 1973-09-25 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB1479902A true GB1479902A (en) | 1977-07-13 |
Family
ID=23584830
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB41450/74A Expired GB1479902A (en) | 1973-09-25 | 1974-09-24 | Esters and amides of trisubstituted hydroxyphenylalkanoic acids |
Country Status (9)
Country | Link |
---|---|
JP (1) | JPS5060479A (enrdf_load_stackoverflow) |
BE (1) | BE820263A (enrdf_load_stackoverflow) |
DE (1) | DE2445345A1 (enrdf_load_stackoverflow) |
DK (1) | DK502374A (enrdf_load_stackoverflow) |
FR (1) | FR2244748B1 (enrdf_load_stackoverflow) |
GB (1) | GB1479902A (enrdf_load_stackoverflow) |
LU (1) | LU70972A1 (enrdf_load_stackoverflow) |
NL (1) | NL7412674A (enrdf_load_stackoverflow) |
ZA (1) | ZA745383B (enrdf_load_stackoverflow) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115716912A (zh) * | 2022-11-04 | 2023-02-28 | 万华化学集团股份有限公司 | 一种耐黄变热塑性树脂组合物及其制备方法和应用 |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1522477A (en) * | 1974-08-13 | 1978-08-23 | Ici Ltd | Process for the manufacture of rho-hydroxybenzyl cyanide |
GB1576332A (en) * | 1976-03-01 | 1980-10-08 | Ici Ltd | Process for the manufacture of p-hydroxybenzyl cyanide |
AU522277B2 (en) * | 1978-08-04 | 1982-05-27 | Uniroyal Chemical Company, Inc. | Phenolic esteramides |
US4434122A (en) * | 1982-05-11 | 1984-02-28 | Phillips Petroleum Company | Polymer stabilization |
AU573647B2 (en) * | 1984-01-30 | 1988-06-16 | General Electric Company | Uv-stabilised polymer compositions |
US4598113A (en) * | 1985-08-15 | 1986-07-01 | Ici Americas Inc. | Hindered hydroxyphenylalkanoates of ethoxylated bisphenol A and stabilized compositions |
JPH07728B2 (ja) * | 1987-05-20 | 1995-01-11 | 三ツ星ベルト株式会社 | ポリアセタ−ル樹脂組成物 |
JP2525452B2 (ja) * | 1988-04-27 | 1996-08-21 | 東レ株式会社 | 熱安定性に優れたポリアセタ―ル樹脂組成物 |
KR910016673A (ko) * | 1990-03-30 | 1991-11-05 | 베르너 발데크 | 히드록시페닐프로피오네이트의 제조방법 |
JP5596327B2 (ja) * | 2009-01-28 | 2014-09-24 | 株式会社Adeka | 食品・医療・水道用パイプ用途のポリオレフィン系樹脂組成物 |
JP6196777B2 (ja) * | 2013-01-22 | 2017-09-13 | 株式会社Adeka | 潤滑油用酸化防止剤組成物及びそれを含有する潤滑油組成物 |
-
1974
- 1974-08-21 ZA ZA00745383A patent/ZA745383B/xx unknown
- 1974-09-23 DE DE19742445345 patent/DE2445345A1/de not_active Withdrawn
- 1974-09-23 LU LU70972A patent/LU70972A1/xx unknown
- 1974-09-24 FR FR7432110A patent/FR2244748B1/fr not_active Expired
- 1974-09-24 DK DK502374A patent/DK502374A/da unknown
- 1974-09-24 GB GB41450/74A patent/GB1479902A/en not_active Expired
- 1974-09-24 BE BE148823A patent/BE820263A/xx unknown
- 1974-09-25 NL NL7412674A patent/NL7412674A/xx unknown
- 1974-09-25 JP JP49110362A patent/JPS5060479A/ja active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115716912A (zh) * | 2022-11-04 | 2023-02-28 | 万华化学集团股份有限公司 | 一种耐黄变热塑性树脂组合物及其制备方法和应用 |
CN115716912B (zh) * | 2022-11-04 | 2023-09-19 | 万华化学集团股份有限公司 | 一种耐黄变热塑性树脂组合物及其制备方法和应用 |
Also Published As
Publication number | Publication date |
---|---|
ZA745383B (en) | 1975-09-24 |
FR2244748B1 (enrdf_load_stackoverflow) | 1976-12-31 |
LU70972A1 (enrdf_load_stackoverflow) | 1975-06-16 |
DE2445345A1 (de) | 1975-03-27 |
NL7412674A (nl) | 1975-03-27 |
FR2244748A1 (enrdf_load_stackoverflow) | 1975-04-18 |
DK502374A (enrdf_load_stackoverflow) | 1975-05-26 |
JPS5060479A (enrdf_load_stackoverflow) | 1975-05-24 |
BE820263A (fr) | 1975-03-24 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PS | Patent sealed | ||
PCNP | Patent ceased through non-payment of renewal fee |