GB976939A - Production of pyrrolidone - Google Patents
Production of pyrrolidoneInfo
- Publication number
- GB976939A GB976939A GB4021362A GB4021362A GB976939A GB 976939 A GB976939 A GB 976939A GB 4021362 A GB4021362 A GB 4021362A GB 4021362 A GB4021362 A GB 4021362A GB 976939 A GB976939 A GB 976939A
- Authority
- GB
- United Kingdom
- Prior art keywords
- catalysts
- sintered
- catalyst
- ammonia
- acid
- 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
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 title abstract 4
- 239000003054 catalyst Substances 0.000 abstract 12
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 abstract 10
- 229910021529 ammonia Inorganic materials 0.000 abstract 5
- 150000001875 compounds Chemical class 0.000 abstract 5
- 230000008018 melting Effects 0.000 abstract 5
- 238000002844 melting Methods 0.000 abstract 5
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 abstract 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 abstract 4
- 239000000956 alloy Substances 0.000 abstract 4
- 229910045601 alloy Inorganic materials 0.000 abstract 4
- 229910017052 cobalt Inorganic materials 0.000 abstract 4
- 239000010941 cobalt Substances 0.000 abstract 4
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 abstract 4
- 238000010438 heat treatment Methods 0.000 abstract 4
- 239000001257 hydrogen Substances 0.000 abstract 4
- 229910052739 hydrogen Inorganic materials 0.000 abstract 4
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 abstract 4
- 239000011976 maleic acid Substances 0.000 abstract 4
- 229910052751 metal Inorganic materials 0.000 abstract 4
- 239000002184 metal Substances 0.000 abstract 4
- 239000000203 mixture Substances 0.000 abstract 4
- 238000002360 preparation method Methods 0.000 abstract 4
- KDYFGRWQOYBRFD-UHFFFAOYSA-N succinic acid Chemical compound OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 abstract 4
- 239000002253 acid Substances 0.000 abstract 3
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 abstract 2
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 abstract 2
- 150000007513 acids Chemical class 0.000 abstract 2
- 150000003863 ammonium salts Chemical class 0.000 abstract 2
- NHJPVZLSLOHJDM-UHFFFAOYSA-N azane;butanedioic acid Chemical compound [NH4+].[NH4+].[O-]C(=O)CCC([O-])=O NHJPVZLSLOHJDM-UHFFFAOYSA-N 0.000 abstract 2
- 229910052793 cadmium Inorganic materials 0.000 abstract 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 239000000969 carrier Substances 0.000 abstract 2
- 239000004927 clay Substances 0.000 abstract 2
- 229910052802 copper Inorganic materials 0.000 abstract 2
- 239000010949 copper Substances 0.000 abstract 2
- 235000011087 fumaric acid Nutrition 0.000 abstract 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract 2
- 239000007791 liquid phase Substances 0.000 abstract 2
- 229910052748 manganese Inorganic materials 0.000 abstract 2
- 239000011572 manganese Substances 0.000 abstract 2
- 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 2
- 229910044991 metal oxide Inorganic materials 0.000 abstract 2
- 150000004706 metal oxides Chemical class 0.000 abstract 2
- 150000002739 metals Chemical class 0.000 abstract 2
- 229910052759 nickel Inorganic materials 0.000 abstract 2
- 239000003960 organic solvent Substances 0.000 abstract 2
- 239000008262 pumice Substances 0.000 abstract 2
- 150000003839 salts Chemical class 0.000 abstract 2
- 150000004760 silicates Chemical class 0.000 abstract 2
- 229910052709 silver Inorganic materials 0.000 abstract 2
- 239000004332 silver Substances 0.000 abstract 2
- 238000005245 sintering Methods 0.000 abstract 2
- -1 succinic acid, amide ammonium salt Chemical class 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 abstract 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 abstract 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 abstract 1
- 150000004292 cyclic ethers Chemical class 0.000 abstract 1
- CKKXWJDFFQPBQL-UAIGNFCESA-N diazanium;(z)-but-2-enedioate Chemical compound [NH4+].[NH4+].[O-]C(=O)\C=C/C([O-])=O CKKXWJDFFQPBQL-UAIGNFCESA-N 0.000 abstract 1
- 239000001530 fumaric acid Substances 0.000 abstract 1
- 150000002238 fumaric acids Chemical class 0.000 abstract 1
- 150000004679 hydroxides Chemical class 0.000 abstract 1
- 239000011261 inert gas Substances 0.000 abstract 1
- 229910052742 iron Inorganic materials 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 150000002689 maleic acids Chemical class 0.000 abstract 1
- 230000007935 neutral effect Effects 0.000 abstract 1
- 229910000480 nickel oxide Inorganic materials 0.000 abstract 1
- 150000002823 nitrates Chemical class 0.000 abstract 1
- 150000002826 nitrites Chemical class 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- GNRSAWUEBMWBQH-UHFFFAOYSA-N oxonickel Chemical compound [Ni]=O GNRSAWUEBMWBQH-UHFFFAOYSA-N 0.000 abstract 1
- 239000008188 pellet Substances 0.000 abstract 1
- 239000011541 reaction mixture Substances 0.000 abstract 1
- 229930195734 saturated hydrocarbon Natural products 0.000 abstract 1
- 239000001384 succinic acid Substances 0.000 abstract 1
- 150000003444 succinic acids Chemical class 0.000 abstract 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/70—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
- B01J23/74—Iron group metals
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J23/00—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
- B01J23/90—Regeneration or reactivation
Landscapes
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
Pyrrolidone is made by the reaction in the liquid phase of a compound of the formula HOOC-A-COOH, where A represents -CH2-CH2-or-CH=CH -with ammonia and hydrogen at 150-280 DEG C. and at a pressure of 20-400 atmospheres in the presence of sintered Co, Ni, Cu and/or Fe as a catalyst. The catalysts (see Division B1) which may be supported on carriers, e.g. pumice, clay or silicates, may be used singly or as mixtures or alloys of two, three or all of the metals and may also contain manganese, silver or cadmium, either singly or in admixture with one another. The catalysts are sintered by heating to slightly, e.g., 20-80 DEG C., below the melting point of the metal, the lowest melting component of a mixture or of the alloy. Particularly active catalysts are obtained from sintering metal oxides, or compounds which can be converted into oxides on heating, at temperatures preferably above 1000 DEG C. and subsequently hydrogenating, preferably at 250-400 DEG C. Suitable dibasic acids are succinic, maleic and fumaric acids. The ammonia, preferably in 5-20 molar excess of the diacid, may be added in the gaseous or liquid state or dissolved in water and/or an inert organic solvent, e.g. cyclic ethers. In the former two instances it is usual to add 60-90%, by weight of diacid, of water and/or organic solvent to the reaction mixture. Alternatively the ammonia can be combined with the diacid as, e.g. the acid or neutral salt, the monoamide of succinic acid or maleic acid or the ammonium salts thereof, or as the diamide of the unsaturated acids, preferably with additional free ammonia. The hydrogen may be diluted with an inert gas, e.g. nitrogen or saturated hydrocarbons. The reaction is carried out for, e.g. 5-25 hours, at temperatures between 150-280 DEG C., preferbly 170-250 DEG C. and particularly 190-230 DEG C. and at hydrogen pressures of 20-400, preferably 45-250 atmospheres. Examples describe the preparation of pyrrolidone using a cobalt catalyst with diammonium succinate, succinic acid, amide ammonium salt of succinic acid, maleic acid; ammonium salt of maleic acid, ammonium amide salt of maleic acid and the diammonium salt of fumaric acid, a nickel catalyst and diammonium succinate and a cobalt/manganese catalyst and ammonium maleate.ALSO:Sintered Co, Ni, Cu and Fe, or mixtures or alloys of two, three or all of these metals are used as catalysts in the preparation of pyrrolidone from a compound HOOC-A-COOH, in which A is -CH2-CH2- or -CH=CH-, ammonia and hydrogen in the liquid phase. The catalysts can also contain manganese, silver and/or cadmium and may be supported on carriers, e.g. pumice, clay or silicates, which can amount to 50-95% by weight of the total suported catalyst. The catalysts are sintered by heating to slightly, e.g. 20-80 DEG C., below the melting point of the metal, the lowest melting component of a mixture or of the alloy. Particularly active catalysts are obtained by sintering the metal oxide, or compounds which can be converted into oxides on heating, e.g. hydroxides, carbonates, nitrates or nitrites, at temperatures preferably above 1000 DEG C., but 20 DEG C. below the melting point of the compound. The oxide is subsequently reduced at temperatures between 150-600 DEG C. Example 1 describes the preparation of sintered cobalt in pellet form, Example 5 describes the reduction of sintered nickel oxide, and Example 2 describes the preparation of a cobalt/manganese catalyst.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DEB64578A DE1204674B (en) | 1961-10-28 | 1961-10-28 | Process for the preparation of pyrrolidone |
| DEB64646A DE1205544B (en) | 1961-11-03 | 1961-11-03 | Process for the preparation of pyrrolidone |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB976939A true GB976939A (en) | 1964-12-02 |
Family
ID=25966065
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4021362A Expired GB976939A (en) | 1961-10-28 | 1962-10-24 | Production of pyrrolidone |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB976939A (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4036836A (en) * | 1975-06-30 | 1977-07-19 | Standard Oil Company | Process for producing 2-pyrrolidone |
| EP0027022A1 (en) * | 1979-10-05 | 1981-04-15 | The Standard Oil Company | Production of five-membered nitrogen-containing saturated heterocyclic compounds and catalyst suitable therefor |
| US4814464A (en) * | 1987-03-30 | 1989-03-21 | Amoco Corporation | Process for making N-alkylpyrrolidones |
| US4885371A (en) * | 1989-06-22 | 1989-12-05 | Gaf Chemicals Corporation | Process for the preparation of purified N-alkyl lactams |
| US7427684B2 (en) | 2003-10-30 | 2008-09-23 | Davy Process Technology Limited | Process for the production of lactams |
-
1962
- 1962-10-24 GB GB4021362A patent/GB976939A/en not_active Expired
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4036836A (en) * | 1975-06-30 | 1977-07-19 | Standard Oil Company | Process for producing 2-pyrrolidone |
| EP0027022A1 (en) * | 1979-10-05 | 1981-04-15 | The Standard Oil Company | Production of five-membered nitrogen-containing saturated heterocyclic compounds and catalyst suitable therefor |
| US4814464A (en) * | 1987-03-30 | 1989-03-21 | Amoco Corporation | Process for making N-alkylpyrrolidones |
| US4885371A (en) * | 1989-06-22 | 1989-12-05 | Gaf Chemicals Corporation | Process for the preparation of purified N-alkyl lactams |
| US7427684B2 (en) | 2003-10-30 | 2008-09-23 | Davy Process Technology Limited | Process for the production of lactams |
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