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GB976939A - Production of pyrrolidone - Google Patents

Production of pyrrolidone

Info

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
Application number
GB4021362A
Inventor
Walter Himmele
Nikolaus Von Kutepow
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
BASF SE
Original Assignee
BASF SE
Badische Anilin and Sodafabrik AG
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Priority claimed from DEB64578A external-priority patent/DE1204674B/en
Priority claimed from DEB64646A external-priority patent/DE1205544B/en
Application filed by BASF SE, Badische Anilin and Sodafabrik AG filed Critical BASF SE
Publication of GB976939A publication Critical patent/GB976939A/en
Expired legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/70Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper
    • B01J23/74Iron group metals
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J23/00Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00
    • B01J23/90Regeneration 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.
GB4021362A 1961-10-28 1962-10-24 Production of pyrrolidone Expired GB976939A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (5)

* Cited by examiner, † Cited by third party
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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