GB1313286A - Aminoacetols and aminoketals processes for their manufacture and their use - Google Patents
Aminoacetols and aminoketals processes for their manufacture and their useInfo
- Publication number
- GB1313286A GB1313286A GB1055071*[A GB1055071A GB1313286A GB 1313286 A GB1313286 A GB 1313286A GB 1055071 A GB1055071 A GB 1055071A GB 1313286 A GB1313286 A GB 1313286A
- Authority
- GB
- United Kingdom
- Prior art keywords
- converted
- cyanoethyl
- reaction
- ethyleneglycol
- acetal
- 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
- 238000004519 manufacturing process Methods 0.000 title 1
- 238000000034 method Methods 0.000 title 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract 12
- 229940093476 ethylene glycol Drugs 0.000 abstract 5
- -1 Aminoalkyl acetals Chemical class 0.000 abstract 4
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 abstract 4
- 238000006243 chemical reaction Methods 0.000 abstract 4
- 125000001931 aliphatic group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 abstract 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 abstract 2
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 abstract 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 abstract 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 abstract 2
- 239000003795 chemical substances by application Substances 0.000 abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 2
- PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 abstract 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000001731 2-cyanoethyl group Chemical group [H]C([H])(*)C([H])([H])C#N 0.000 abstract 1
- JEQZAEPYFGSAIF-UHFFFAOYSA-N 4-acetyl-4-(2-cyanoethyl)heptanedinitrile Chemical compound N#CCCC(C(=O)C)(CCC#N)CCC#N JEQZAEPYFGSAIF-UHFFFAOYSA-N 0.000 abstract 1
- XWNSFEAWWGGSKJ-UHFFFAOYSA-N 4-acetyl-4-methylheptanedinitrile Chemical compound N#CCCC(C)(C(=O)C)CCC#N XWNSFEAWWGGSKJ-UHFFFAOYSA-N 0.000 abstract 1
- JETVJXLQFOJCBK-UHFFFAOYSA-N 4-formyl-4-methylheptanedinitrile Chemical compound N#CCCC(C)(CCC#N)C=O JETVJXLQFOJCBK-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000004146 Propane-1,2-diol Substances 0.000 abstract 1
- 239000007983 Tris buffer Substances 0.000 abstract 1
- 125000002777 acetyl group Chemical class [H]C([H])([H])C(*)=O 0.000 abstract 1
- 150000001298 alcohols Chemical class 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 1
- 239000003822 epoxy resin Substances 0.000 abstract 1
- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 abstract 1
- 150000002431 hydrogen Chemical class 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 229920000647 polyepoxide Polymers 0.000 abstract 1
- 229960004063 propylene glycol Drugs 0.000 abstract 1
- 235000013772 propylene glycol Nutrition 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/12—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms
- C07D303/18—Compounds containing oxirane rings with hydrocarbon radicals, substituted by singly or doubly bound oxygen atoms by etherified hydroxyl radicals
- C07D303/20—Ethers with hydroxy compounds containing no oxirane rings
- C07D303/24—Ethers with hydroxy compounds containing no oxirane rings with polyhydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/28—Radicals substituted by nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G59/00—Polycondensates containing more than one epoxy group per molecule; Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups
- C08G59/18—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing
- C08G59/40—Macromolecules obtained by polymerising compounds containing more than one epoxy group per molecule using curing agents or catalysts which react with the epoxy groups ; e.g. general methods of curing characterised by the curing agents used
- C08G59/50—Amines
- C08G59/504—Amines containing an atom other than nitrogen belonging to the amine group, carbon and hydrogen
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)
- Epoxy Resins (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH603170A CH556819A (de) | 1970-04-22 | 1970-04-22 | Verfahren zur herstellung von neuen aminoacetalen und aminoketalen, und ihre anwendung. |
| US13577471A | 1971-04-20 | 1971-04-20 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1313286A true GB1313286A (en) | 1973-04-11 |
Family
ID=25698862
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB1055071*[A Expired GB1313286A (en) | 1970-04-22 | 1971-04-21 | Aminoacetols and aminoketals processes for their manufacture and their use |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3714196A (enExample) |
| CH (1) | CH556819A (enExample) |
| DE (1) | DE2119689A1 (enExample) |
| FR (1) | FR2089981A5 (enExample) |
| GB (1) | GB1313286A (enExample) |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH572460A5 (enExample) * | 1972-07-28 | 1976-02-13 | Ciba Geigy Ag | |
| US4365073A (en) * | 1980-10-20 | 1982-12-21 | The Dow Chemical Company | Derivatives of cyano-substituted ketones and aldehydes |
| US4483995A (en) * | 1982-03-11 | 1984-11-20 | International Flavors & Fragrances Inc. | Process for producing solanone, norsolanadione and intermediates therefor |
| US4600763A (en) * | 1985-09-05 | 1986-07-15 | Ashland Oil, Inc. | Interpolymers of bicyclic amide acetals/dicarboxylic acid anhydrides/polyepoxides |
| WO2013155173A2 (en) * | 2012-04-13 | 2013-10-17 | Regents Of The University Of Minnesota | Methods and compositions relating to biodegradable epoxy elastomers |
| CN103242509B (zh) * | 2013-04-18 | 2015-06-10 | 艾达索高新材料无锡有限公司 | 可降解环缩醛、环缩酮二胺类环氧树脂固化剂及其应用 |
-
1970
- 1970-04-22 CH CH603170A patent/CH556819A/xx not_active IP Right Cessation
-
1971
- 1971-04-20 US US00135774A patent/US3714196A/en not_active Expired - Lifetime
- 1971-04-21 GB GB1055071*[A patent/GB1313286A/en not_active Expired
- 1971-04-21 FR FR7114128A patent/FR2089981A5/fr not_active Expired
- 1971-04-22 DE DE19712119689 patent/DE2119689A1/de active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| CH556819A (de) | 1974-12-13 |
| DE2119689A1 (de) | 1971-12-30 |
| FR2089981A5 (enExample) | 1972-01-07 |
| US3714196A (en) | 1973-01-30 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |