GB1457062A

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

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Publication
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US3597481A
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Heterogeneous catalyst for the liquid phase hydrolysis of nitriles to amides

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(en)

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Manufacture of carboxylic acid amides

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(en)

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(en)

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(en)

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A process for activating phosphate dehydration catalysts, and a phosphate dehydration catalyst

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(en)

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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

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