GB1457062A – Manufacture of carboxylic acid amides
– Google Patents
GB1457062A – Manufacture of carboxylic acid amides
– Google Patents
Manufacture of carboxylic acid amides
Info
Publication number
GB1457062A
GB1457062A
GB1692274A
GB1692274A
GB1457062A
GB 1457062 A
GB1457062 A
GB 1457062A
GB 1692274 A
GB1692274 A
GB 1692274A
GB 1692274 A
GB1692274 A
GB 1692274A
GB 1457062 A
GB1457062 A
GB 1457062A
Authority
GB
United Kingdom
Prior art keywords
ene
hydration
nitrile
amides
adiponitrile
Prior art date
1973-04-19
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
GB1692274A
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
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.)
1973-04-19
Filing date
1974-04-18
Publication date
1976-12-01
1974-04-18
Application filed by BASF SE
filed
Critical
BASF SE
1976-12-01
Publication of GB1457062A
publication
Critical
patent/GB1457062A/en
Status
Expired
legal-status
Critical
Current
Links
Espacenet
Global Dossier
Discuss
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
B01J23/12—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of actinides
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
B01J23/76—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 – B01J23/36
B01J23/84—Catalysts comprising metals or metal oxides or hydroxides, not provided for in group B01J21/00 of the iron group metals or copper combined with metals, oxides or hydroxides provided for in groups B01J23/02 – B01J23/36 with arsenic, antimony, bismuth, vanadium, niobium, tantalum, polonium, chromium, molybdenum, tungsten, manganese, technetium or rhenium
Abstract
1457062 Hydration of nitriles to amides BASF AG 18 April 1974 [19 April 1973] 16922/74 Heading C2C [Also in Division B1] Amides are produced by the addition of water to nitriles in the presence of a catalyst containing copper and magnesium silicate and formed by precipitation of magnesium in the presence of a copper compound using alkali metal silicate and then treating with a reducing gas at elevated temperature. The nitrile may be of the formula R(CN) x where x is 1 or 2 and R is substituted or unsubstituted C 1 to C 6 alkyl- (ene), C 2 to C 6 alkenyl(ene), C 5 or C 6 cycloalkyl- (ene), C 7 to C 12 aralkyl(ene), phenyl(ene) or naphthyl(ene) wherein the suffix “ene” refers to the case when x is 2. The hydration may be carried out with a ratio of 1 to 50 moles water per mole of nitrile group of the feed, a temperature of 50-150‹ C., and atmospheric or superatmospheric pressure. Specified nitrile feeds are: acetonitrile, propionitrile, cyclohexanonitrile, adiponitrile, acrylonitrile, methacrylonitrile, crotononitrile, beta-phenylacrylonitrile, benzonitrile, p-toluonitrile, alpha-naphthonitrile, phthalodinitrile, terephthalodinitrile, isophthalodinitrile, butyronitrile, maleodinitrile, glutarodinitrile, succinodinitrile, valeronitrile, capronitrile, fumarodinitrile, beta-phenylacetonitrile and p-ethoxybenzonitrile. The examples describe hydration of acrylonitrile to acrylamide, methacrylonitrile to methacrylamide, benzonitrile to benzamide, adiponitrile to adipodiamide and acetonitrile to acetamide.
GB1692274A
1973-04-19
1974-04-18
Manufacture of carboxylic acid amides
Expired
GB1457062A
(en)
Applications Claiming Priority (1)
Application Number
Priority Date
Filing Date
Title
DE2320060A
DE2320060C2
(en)
1973-04-19
1973-04-19
Process for the preparation of carboxamides
Publications (1)
Publication Number
Publication Date
GB1457062A
true
GB1457062A
(en)
1976-12-01
Family
ID=5878742
Family Applications (1)
Application Number
Title
Priority Date
Filing Date
GB1692274A
Expired
GB1457062A
(en)
1973-04-19
1974-04-18
Manufacture of carboxylic acid amides
Country Status (14)
Country
Link
US
(1)
US3928439A
(en)
JP
(1)
JPS5831334B2
(en)
AT
(1)
AT336560B
(en)
BE
(1)
BE813973A
(en)
BR
(1)
BR7403189D0
(en)
CA
(1)
CA1020951A
(en)
CH
(1)
CH590208A5
(en)
DE
(1)
DE2320060C2
(en)
FR
(1)
FR2226386B1
(en)
GB
(1)
GB1457062A
(en)
IT
(1)
IT1006490B
(en)
NL
(1)
NL180659C
(en)
SU
(1)
SU560529A3
(en)
ZA
(1)
ZA742464B
(en)
Families Citing this family (5)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
US4163735A
(en)
*
1977-07-25
1979-08-07
American Cyanamid Company
Catalyst preparation method
DE2751336A1
(en)
*
1977-11-17
1979-05-23
Basf Ag
PROCESS FOR THE PRODUCTION OF CARBONIC ACID AMIDES
HU207672B
(en)
*
1989-09-18
1993-05-28
Mta Koezponti Kemiai Kutato In
Method for producing catalyzer and producing acid amides by applying the same
DE4221604A1
(en)
*
1992-07-01
1994-01-05
Basf Ag
Process for the preparation of 5-cyanvaleric acid amide
DE102008001319A1
(en)
*
2008-04-22
2009-10-29
Evonik Röhm Gmbh
Catalyst for the conversion of carbonitriles
Family Cites Families (5)
* Cited by examiner, † Cited by third party
Publication number
Priority date
Publication date
Assignee
Title
US1738971A
(en)
*
1927-08-02
1929-12-10
Roessler & Hasslacher Chemical
Process and catalyst for synthesis of methanol
US3597481A
(en)
*
1969-01-16
1971-08-03
Dow Chemical Co
Heterogeneous catalyst for the liquid phase hydrolysis of nitriles to amides
US3642894A
(en)
*
1969-12-05
1972-02-15
Dow Chemical Co
Catalysts for the hydration of nitriles to amides
US3642643A
(en)
*
1969-12-15
1972-02-15
Dow Chemical Co
Regeneration of copper oxide and copper chromite catalysts
US3696152A
(en)
*
1970-06-17
1972-10-03
Dow Chemical Co
Hydration of nitriles to amides using heterogeneous cupreous catalysts
1973
1973-04-19
DE
DE2320060A
patent/DE2320060C2/en
not_active
Expired
1974
1974-04-10
US
US459458A
patent/US3928439A/en
not_active
Expired – Lifetime
1974-04-11
CA
CA197,526A
patent/CA1020951A/en
not_active
Expired
1974-04-16
CH
CH520674A
patent/CH590208A5/xx
not_active
IP Right Cessation
1974-04-17
IT
IT21557/74A
patent/IT1006490B/en
active
1974-04-17
SU
SU2017621A
patent/SU560529A3/en
active
1974-04-17
NL
NLAANVRAGE7405206,A
patent/NL180659C/en
not_active
IP Right Cessation
1974-04-18
AT
AT321674A
patent/AT336560B/en
not_active
IP Right Cessation
1974-04-18
GB
GB1692274A
patent/GB1457062A/en
not_active
Expired
1974-04-18
ZA
ZA00742464A
patent/ZA742464B/en
unknown
1974-04-18
JP
JP49042781A
patent/JPS5831334B2/en
not_active
Expired
1974-04-19
BR
BR3189/74A
patent/BR7403189D0/en
unknown
1974-04-19
BE
BE143431A
patent/BE813973A/en
not_active
IP Right Cessation
1974-04-19
FR
FR7413807A
patent/FR2226386B1/fr
not_active
Expired
Also Published As
Publication number
Publication date
US3928439A
(en)
1975-12-23
DE2320060C2
(en)
1982-10-14
BR7403189D0
(en)
1974-12-24
AU6784074A
(en)
1975-10-16
CA1020951A
(en)
1977-11-15
AT336560B
(en)
1977-05-10
NL180659C
(en)
1990-06-18
FR2226386A1
(en)
1974-11-15
IT1006490B
(en)
1976-09-30
NL180659B
(en)
1986-11-03
JPS5831334B2
(en)
1983-07-05
ATA321674A
(en)
1976-09-15
NL7405206A
(en)
1974-10-22
FR2226386B1
(en)
1977-10-14
ZA742464B
(en)
1975-05-28
BE813973A
(en)
1974-10-21
SU560529A3
(en)
1977-05-30
DE2320060A1
(en)
1974-11-07
JPS5012001A
(en)
1975-02-07
CH590208A5
(en)
1977-07-29
Similar Documents
Publication
Publication Date
Title
US3597481A
(en)
1971-08-03
Heterogeneous catalyst for the liquid phase hydrolysis of nitriles to amides
US3381034A
(en)
1968-04-30
Process for hydrolyzing nitriles
GB1457062A
(en)
1976-12-01
Manufacture of carboxylic acid amides
EP0040896B1
(en)
1984-04-25
Synthesis of amides
GB1370018A
(en)
1974-10-09
Regeneration of catalysts for hydration of nitrile compounds
GB1417026A
(en)
1975-12-10
Process for hydrating an unsaturated nitrile
JPS56131555A
(en)
1981-10-15
Preparation of n-substituted acrylamide or n-substituted methacrylamide
US4176137A
(en)
1979-11-27
Manufacture of carboxylic acid amides
US3789074A
(en)
1974-01-29
Particle size-ph effects on reduced copper oxide in preparation of acrylamide
GB1157441A
(en)
1969-07-09
Reductive Dimerisation of Unsaturated Nitriles
CA1241020A
(en)
1988-08-23
Simultaneous preparation of nitriles and acrylamide or methacrylamide
US4365091A
(en)
1982-12-21
Method for the production of acrylamide
US5434291A
(en)
1995-07-18
Preparation of aminopropionitriles
US2798882A
(en)
1957-07-09
Preparation of acrylonitrile
GB1459685A
(en)
1976-12-22
Conversion of nitriles to amides
GB2023143A
(en)
1979-12-28
Continuous Cyanoethylation Process
US3114764A
(en)
1963-12-17
Acrylonitrile synthesis from acetylene and hydrogen cyanide in non-aqueous promoted cuprous chloride catalyst solution
GB831831A
(en)
1960-04-06
A process for activating phosphate dehydration catalysts, and a phosphate dehydration catalyst
ATE55766T1
(en)
1990-09-15
HYDRATION PROCESSES OF NITRILE COMPOUNDS.
US2999072A
(en)
1961-09-05
Catalyst for acrylonitrile synthesis
US4574157A
(en)
1986-03-04
Process for preparing anhydrous cyclic imido esters
US3340207A
(en)
1967-09-05
Catalyst composition
USRE28525E
(en)
1975-08-19
Process for hydrolyzing nitriles
TW363956B
(en)
1999-07-11
Process for preparing p-nitroaromatic amides and products thereof
US4921969A
(en)
1990-05-01
Method for the preparation of imidazoles
Legal Events
Date
Code
Title
Description
1977-04-14
PS
Patent sealed [section 19, patents act 1949]
1994-05-18
PE20
Patent expired after termination of 20 years
Effective date:
19940417