ES255246A1 - Proceso de nitraciën de metil 2-furil cetona para producir metil 5-nitro-2-furil cetona, que incluye el tratamiento de la metil 2-furil cetona con una mezcla nitradora formada por acido nitrico y anhidrico acetico para formar un intermedio de nitraci - Google Patents
Proceso de nitraciën de metil 2-furil cetona para producir metil 5-nitro-2-furil cetona, que incluye el tratamiento de la metil 2-furil cetona con una mezcla nitradora formada por acido nitrico y anhidrico acetico para formar un intermedio de nitraciInfo
- Publication number
- ES255246A1 ES255246A1 ES0255246A ES255246A ES255246A1 ES 255246 A1 ES255246 A1 ES 255246A1 ES 0255246 A ES0255246 A ES 0255246A ES 255246 A ES255246 A ES 255246A ES 255246 A1 ES255246 A1 ES 255246A1
- Authority
- ES
- Spain
- Prior art keywords
- nitro
- furyl ketone
- methyl
- treating
- water
- 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
- YIUZDGLJEZOSGS-UHFFFAOYSA-N bis(3-methyl-5-nitrofuran-2-yl)methanone Chemical compound CC1=C(OC(=C1)[N+](=O)[O-])C(=O)C=1OC(=CC=1C)[N+](=O)[O-] YIUZDGLJEZOSGS-UHFFFAOYSA-N 0.000 title abstract 2
- WFDIJRYMOXRFFG-UHFFFAOYSA-N Acetic anhydride Chemical compound CC(=O)OC(C)=O WFDIJRYMOXRFFG-UHFFFAOYSA-N 0.000 abstract 3
- 239000002253 acid Substances 0.000 abstract 2
- 238000006396 nitration reaction Methods 0.000 abstract 2
- SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- IEMMBWWQXVXBEU-UHFFFAOYSA-N 2-acetylfuran Chemical compound CC(=O)C1=CC=CO1 IEMMBWWQXVXBEU-UHFFFAOYSA-N 0.000 abstract 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 238000010790 dilution Methods 0.000 abstract 1
- 239000012895 dilution Substances 0.000 abstract 1
- 150000007529 inorganic bases Chemical class 0.000 abstract 1
- 229910052500 inorganic mineral Inorganic materials 0.000 abstract 1
- 239000011707 mineral Substances 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 239000012452 mother liquor Substances 0.000 abstract 1
- 230000000802 nitrating effect Effects 0.000 abstract 1
- 229910017604 nitric acid Inorganic materials 0.000 abstract 1
- 235000011056 potassium acetate Nutrition 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- DUIOPKIIICUYRZ-UHFFFAOYSA-N semicarbazide Chemical compound NNC(N)=O DUIOPKIIICUYRZ-UHFFFAOYSA-N 0.000 abstract 1
- 229910052708 sodium Inorganic materials 0.000 abstract 1
- 239000001632 sodium acetate Substances 0.000 abstract 1
- 235000017281 sodium acetate Nutrition 0.000 abstract 1
- 238000000638 solvent extraction Methods 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/70—Nitro radicals
- C07D307/71—Nitro radicals attached in position 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D307/00—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
- C07D307/02—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings
- C07D307/34—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D307/56—Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D307/70—Nitro radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Furan Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
Proceso de nitración de metil 2-furil cetona para producir metil 5-nitro-2-furil cetona, que incluye el tratamiento de la metil 2-furil cetona con una mezcla nitradora formada por ácido nítrico y anhídrido acético para formar un intermedio de nitración, caracterizado dicho proceso porque la fase de convertir el intermedio de nitración en metil 5-nitro-2-furil cetona comprende el tratamiento de dicho intermedio de nitración con una sal de una base fuerte bajo condiciones anhidras.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US794497A US2976300A (en) | 1959-02-20 | 1959-02-20 | Method of preparing methyl 5-nitro-2-furyl ketone |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES255246A1 true ES255246A1 (es) | 1960-04-01 |
Family
ID=25162798
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES0255246A Expired ES255246A1 (es) | 1959-02-20 | 1960-01-23 | Proceso de nitraciën de metil 2-furil cetona para producir metil 5-nitro-2-furil cetona, que incluye el tratamiento de la metil 2-furil cetona con una mezcla nitradora formada por acido nitrico y anhidrico acetico para formar un intermedio de nitraci |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US2976300A (es) |
| AT (1) | AT215419B (es) |
| BE (1) | BE587682A (es) |
| CH (1) | CH383402A (es) |
| DE (1) | DE1154487B (es) |
| DK (1) | DK95422C (es) |
| ES (1) | ES255246A1 (es) |
| GB (1) | GB904091A (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3164521A (en) * | 1962-08-22 | 1965-01-05 | Norwich Pharma Co | Antimycotic compositions comprising chloromethyl 5-nitro-2-furyl ketone |
| US3723477A (en) * | 1970-05-15 | 1973-03-27 | Morton Norwich Products Inc | 4-fluoro-3-methylphenyl 5-nitro-2-furyl ketone |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2490006A (en) * | 1946-08-16 | 1949-11-29 | Eaton Lab Inc | Process of nitrating furan derivatives |
| US2502114A (en) * | 1947-11-18 | 1950-03-28 | Allied Chem & Dye Corp | Process for preparing mononitrofuran compounds |
| GB679202A (en) * | 1949-11-01 | 1952-09-17 | Eaton Lab Inc | Improvements in or relating to the production of 5-nitrofuran derivatives |
| GB797961A (en) * | 1956-02-14 | 1958-07-09 | Messrs Brocades Stheeman | Improvements in or relating to the manufacture of nitrofuran derivatives |
-
1959
- 1959-02-20 US US794497A patent/US2976300A/en not_active Expired - Lifetime
- 1959-11-26 DE DEN17563A patent/DE1154487B/de active Pending
- 1959-12-09 AT AT892259A patent/AT215419B/de active
-
1960
- 1960-01-23 ES ES0255246A patent/ES255246A1/es not_active Expired
- 1960-02-04 GB GB3984/60A patent/GB904091A/en not_active Expired
- 1960-02-16 BE BE587682A patent/BE587682A/fr unknown
- 1960-02-19 DK DK64760AA patent/DK95422C/da active
- 1960-02-19 CH CH187760A patent/CH383402A/de unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US2976300A (en) | 1961-03-21 |
| CH383402A (de) | 1964-10-31 |
| DE1154487B (de) | 1963-09-19 |
| AT215419B (de) | 1961-06-12 |
| GB904091A (en) | 1962-08-22 |
| BE587682A (fr) | 1960-08-16 |
| DK95422C (da) | 1963-02-25 |
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