ATE160564T1 - Herstellung von 3-dihaloacetyl oxazolidine - Google Patents
Herstellung von 3-dihaloacetyl oxazolidineInfo
- Publication number
- ATE160564T1 ATE160564T1 AT94870150T AT94870150T ATE160564T1 AT E160564 T1 ATE160564 T1 AT E160564T1 AT 94870150 T AT94870150 T AT 94870150T AT 94870150 T AT94870150 T AT 94870150T AT E160564 T1 ATE160564 T1 AT E160564T1
- Authority
- AT
- Austria
- Prior art keywords
- dihaloacetyl
- preparation
- oxazolidine
- carbon atoms
- independently
- Prior art date
Links
- WYNCHZVNFNFDNH-UHFFFAOYSA-N Oxazolidine Chemical compound C1COCN1 WYNCHZVNFNFDNH-UHFFFAOYSA-N 0.000 title 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
- 125000004432 carbon atom Chemical group C* 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical class O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 1
- 150000001299 aldehydes Chemical class 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- 238000009903 catalytic hydrogenation reaction Methods 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 150000004820 halides Chemical class 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 150000002576 ketones Chemical class 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 150000002917 oxazolidines Chemical class 0.000 abstract 1
- 229910052760 oxygen Inorganic materials 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
Classifications
-
- 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
- C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
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)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US08/124,067 US5428172A (en) | 1993-09-21 | 1993-09-21 | Preparation of 3-dihaloacetyl oxazolidines |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE160564T1 true ATE160564T1 (de) | 1997-12-15 |
Family
ID=22412547
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT94870150T ATE160564T1 (de) | 1993-09-21 | 1994-09-20 | Herstellung von 3-dihaloacetyl oxazolidine |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US5428172A (de) |
| EP (1) | EP0648768B1 (de) |
| AT (1) | ATE160564T1 (de) |
| DE (1) | DE69407020T2 (de) |
| DK (1) | DK0648768T3 (de) |
| ES (1) | ES2109656T3 (de) |
| GR (1) | GR3026146T3 (de) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ATE171842T1 (de) | 1994-08-30 | 1998-10-15 | Rohm & Haas | Zusammensetzungen aus phosphosulphonat-herbizide und dichloracetamide-safener und verwendungsmethoden |
| US5560872A (en) * | 1995-05-18 | 1996-10-01 | Lever Brothers Company | Compositions comprising oxazolidine and tetrahydrooxazine amide surfactants |
| CN102617560A (zh) * | 2011-01-30 | 2012-08-01 | 南京理工大学 | 呋喃解草唑的制备方法 |
| CN114989115B (zh) * | 2022-07-01 | 2024-04-30 | 兰升生物科技集团股份有限公司 | α-(硝基甲基)-2-呋喃甲醇的改进合成方法和保持该方法中催化剂活性的方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2157386A (en) * | 1937-08-19 | 1939-05-09 | Purdue Research Foundation | Hydrogenation of nitrohydroxy compounds |
| US2347621A (en) * | 1941-07-12 | 1944-04-25 | Commercial Solvents Corp | Process for reduction of nitro hydroxy compounds |
| US2587572A (en) * | 1949-04-27 | 1952-02-26 | Commercial Solvents Corp | Process for production of amino hydroxy compounds by hydrogenation of nitro hydroxy compounds |
| US3402203A (en) * | 1964-11-19 | 1968-09-17 | Commercial Solvents Corp | Process of preparing n, n-dimethylamino alcohols |
| US3564057A (en) * | 1968-10-07 | 1971-02-16 | Commercial Solvents Corp | Production of alkanolamines |
| US3859292A (en) * | 1972-08-15 | 1975-01-07 | Scm Corp | N-haloacyl (2-spirocycloaliphatic) oxazolidines |
| US4038284A (en) * | 1975-07-28 | 1977-07-26 | Stauffer Chemical Company | N-acylation of oxazolidines |
| GB1538318A (en) * | 1976-08-09 | 1979-01-17 | Stauffer Chemical Co | Preparation of n-substituted oxazolidines |
| EP0190105A3 (de) * | 1985-01-31 | 1988-10-26 | Ciba-Geigy Ag | Herbizides Mittel |
-
1993
- 1993-09-21 US US08/124,067 patent/US5428172A/en not_active Expired - Lifetime
-
1994
- 1994-09-20 ES ES94870150T patent/ES2109656T3/es not_active Expired - Lifetime
- 1994-09-20 DE DE69407020T patent/DE69407020T2/de not_active Expired - Fee Related
- 1994-09-20 AT AT94870150T patent/ATE160564T1/de not_active IP Right Cessation
- 1994-09-20 DK DK94870150.3T patent/DK0648768T3/da active
- 1994-09-20 EP EP94870150A patent/EP0648768B1/de not_active Expired - Lifetime
-
1998
- 1998-02-12 GR GR980400320T patent/GR3026146T3/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US5428172A (en) | 1995-06-27 |
| DE69407020D1 (de) | 1998-01-08 |
| DK0648768T3 (da) | 1997-12-29 |
| DE69407020T2 (de) | 1998-06-10 |
| EP0648768A1 (de) | 1995-04-19 |
| EP0648768B1 (de) | 1997-11-26 |
| ES2109656T3 (es) | 1998-01-16 |
| GR3026146T3 (en) | 1998-05-29 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| UEP | Publication of translation of european patent specification | ||
| REN | Ceased due to non-payment of the annual fee |