GB1383106A - Process for the manufacture of cyclic imide-acid esters - Google Patents
Process for the manufacture of cyclic imide-acid estersInfo
- Publication number
- GB1383106A GB1383106A GB2583572A GB2583572A GB1383106A GB 1383106 A GB1383106 A GB 1383106A GB 2583572 A GB2583572 A GB 2583572A GB 2583572 A GB2583572 A GB 2583572A GB 1383106 A GB1383106 A GB 1383106A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- alkyl
- acid esters
- june
- independently
- 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
- 238000000034 method Methods 0.000 title abstract 3
- 239000002253 acid Substances 0.000 title abstract 2
- 125000004122 cyclic group Chemical group 0.000 title abstract 2
- 150000002148 esters Chemical class 0.000 title abstract 2
- 238000004519 manufacturing process Methods 0.000 title 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 3
- -1 substituted cyclo alkyl radical Chemical class 0.000 abstract 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 2
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 239000003054 catalyst Substances 0.000 abstract 2
- KWGKDLIKAYFUFQ-UHFFFAOYSA-M lithium chloride Chemical compound [Li+].[Cl-] KWGKDLIKAYFUFQ-UHFFFAOYSA-M 0.000 abstract 2
- 239000011701 zinc Substances 0.000 abstract 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 abstract 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 abstract 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 abstract 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 150000001414 amino alcohols Chemical class 0.000 abstract 1
- 229910021529 ammonia Inorganic materials 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000005840 aryl radicals Chemical class 0.000 abstract 1
- 229910052793 cadmium Inorganic materials 0.000 abstract 1
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052791 calcium Inorganic materials 0.000 abstract 1
- 239000011575 calcium Substances 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 239000010941 cobalt Substances 0.000 abstract 1
- 229910017052 cobalt Inorganic materials 0.000 abstract 1
- 229910052802 copper Inorganic materials 0.000 abstract 1
- 239000010949 copper Substances 0.000 abstract 1
- 229910052744 lithium Inorganic materials 0.000 abstract 1
- 239000011572 manganese Substances 0.000 abstract 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 abstract 1
- 229910052751 metal Inorganic materials 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 229910052759 nickel Inorganic materials 0.000 abstract 1
- 125000002560 nitrile group Chemical group 0.000 abstract 1
- 150000004893 oxazines Chemical class 0.000 abstract 1
- 150000002918 oxazolines Chemical class 0.000 abstract 1
- 239000012429 reaction media Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229910052725 zinc Inorganic materials 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D265/00—Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
- C07D265/04—1,3-Oxazines; Hydrogenated 1,3-oxazines
- C07D265/06—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings
- C07D265/08—1,3-Oxazines; Hydrogenated 1,3-oxazines not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
- C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
- C07D263/08—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
- C07D263/10—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- C07D263/12—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms with radicals containing only hydrogen and carbon atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19712127776 DE2127776A1 (de) | 1971-06-04 | 1971-06-04 | Verfahren zur Herstellung cyclischer Imidsäureester |
| DE2158061A DE2158061A1 (de) | 1971-06-04 | 1971-11-24 | Verfahren zur herstellung cyclischer imidsaeureester |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1383106A true GB1383106A (en) | 1975-02-05 |
Family
ID=25761233
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB2583572A Expired GB1383106A (en) | 1971-06-04 | 1972-06-02 | Process for the manufacture of cyclic imide-acid esters |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US3813378A (enExample) |
| DE (2) | DE2127776A1 (enExample) |
| FR (1) | FR2141718B1 (enExample) |
| GB (1) | GB1383106A (enExample) |
| IT (1) | IT958179B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2156344A (en) * | 1984-03-26 | 1985-10-09 | Dow Chemical Co | Liquid phase preparation of optionally 2-substituted-2-oxazolines by cyclodehydration |
Families Citing this family (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2329545C2 (de) * | 1973-06-09 | 1986-06-12 | Bayer Ag, 5090 Leverkusen | 1,2-Bis-oxazolinyl-(2)-cyclobutane und Verfahren zu ihrer Herstellung |
| US4061854A (en) * | 1975-06-12 | 1977-12-06 | Shionogi & Co., Ltd. | Dihydroethanoanthracene derivatives useful as antidepressants |
| US4543414A (en) * | 1978-12-05 | 1985-09-24 | The Dow Chemical Company | Liquid phase preparation of 2-substituted-2-oxazolines with cadmium salt catalysts |
| DE3127609A1 (de) * | 1981-07-13 | 1983-01-27 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von n-vinylamiden |
| US4354029A (en) * | 1981-11-30 | 1982-10-12 | The Dow Chemical Company | Preparation of 2-substituted-2-oxazolines with organic zinc salt catalysts |
| DE3224880A1 (de) * | 1982-07-03 | 1984-01-05 | Chemische Werke Hüls AG, 4370 Marl | Verfahren zur herstellung von reinen, wasserfreien imidsaeureestern durch umsetzung von nitrilen mit aminoalkoholen |
| DE3310905A1 (de) * | 1983-03-25 | 1984-09-27 | Henkel KGaA, 4000 Düsseldorf | Verfahren zur herstellung von 2-isopropenyloxazolinen |
| US5227494A (en) * | 1988-09-14 | 1993-07-13 | Schering Corporation | Process for preparing oxazoline compounds |
| DE3914155A1 (de) * | 1989-04-28 | 1990-10-31 | Henkel Kgaa | Verfahren zur herstellung von 5,6-dihydro-4h-1,3-oxazinen |
| CA2094810C (en) * | 1990-10-25 | 2002-06-04 | Jon E. Clark | Process for preparing florfenicol, its analogs and oxazoline intermediates thereto |
| US5773629A (en) * | 1996-06-14 | 1998-06-30 | Industrial Technology Research Institute | Synthesis of (4S, 5R) -2, 4-diphenyl-5-carboxy-oxazoline derivative as taxol side-chain precursor |
| KR101475976B1 (ko) | 2007-07-10 | 2014-12-23 | 스미또모 가가꾸 가부시끼가이샤 | 프로필렌 옥사이드의 제조 방법 |
-
1971
- 1971-06-04 DE DE19712127776 patent/DE2127776A1/de active Pending
- 1971-11-24 DE DE2158061A patent/DE2158061A1/de active Pending
-
1972
- 1972-05-31 IT IT50644/72A patent/IT958179B/it active
- 1972-06-01 FR FR727219657A patent/FR2141718B1/fr not_active Expired
- 1972-06-02 US US00259310A patent/US3813378A/en not_active Expired - Lifetime
- 1972-06-02 GB GB2583572A patent/GB1383106A/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2156344A (en) * | 1984-03-26 | 1985-10-09 | Dow Chemical Co | Liquid phase preparation of optionally 2-substituted-2-oxazolines by cyclodehydration |
Also Published As
| Publication number | Publication date |
|---|---|
| US3813378A (en) | 1974-05-28 |
| IT958179B (it) | 1973-10-20 |
| DE2158061A1 (de) | 1973-05-30 |
| FR2141718A1 (enExample) | 1973-01-26 |
| DE2127776A1 (de) | 1972-12-14 |
| FR2141718B1 (enExample) | 1973-07-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PLE | Entries relating assignments, transmissions, licences in the register of patents | ||
| PLNP | Patent lapsed through nonpayment of renewal fees |