GB1268741A - PREPARATION OF N-ALKYL-alpha,beta-UNSATURATED AMIDE - Google Patents
PREPARATION OF N-ALKYL-alpha,beta-UNSATURATED AMIDEInfo
- Publication number
- GB1268741A GB1268741A GB460470A GB460470A GB1268741A GB 1268741 A GB1268741 A GB 1268741A GB 460470 A GB460470 A GB 460470A GB 460470 A GB460470 A GB 460470A GB 1268741 A GB1268741 A GB 1268741A
- Authority
- GB
- United Kingdom
- Prior art keywords
- alkyl
- preparation
- unsaturated
- reaction
- formula
- 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
- 150000001408 amides Chemical class 0.000 title abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 2
- 238000006243 chemical reaction Methods 0.000 abstract 2
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 239000003054 catalyst Substances 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000002184 metal Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 150000007522 mineralic acids Chemical class 0.000 abstract 1
- PBSASXNAZJHOBR-UHFFFAOYSA-N n-(2-methylpropyl)prop-2-enamide Chemical compound CC(C)CNC(=O)C=C PBSASXNAZJHOBR-UHFFFAOYSA-N 0.000 abstract 1
- 150000002825 nitriles Chemical class 0.000 abstract 1
- 150000007524 organic acids Chemical class 0.000 abstract 1
- 238000010526 radical polymerization reaction Methods 0.000 abstract 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/01—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
- C07C233/02—Carboxylic acid amides having carbon atoms of carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms having nitrogen atoms of carboxamide groups bound to hydrogen atoms or to carbon atoms of unsubstituted hydrocarbon radicals
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
1,268,741. N-alkyl-α,#-unsaturated amides. ASAHI KASEI KOGYO K.K. 30 Jan., 1970 [4 Feb., 1969 (2)], No. 4604/70. Heading C2C. A process for the preparation of an N-alkyl- α,#-unsaturated amide comprises reacting an α,#-unsaturated nitrile of the formula with water and an amine of the formula (R 2 )(R 3 )NH or R 4 NH wherein R 1 and R 2 are hydrogen atoms or alkyl groups, R 3 is an alkyl group and R 4 is a cyclic alkylene group containing 4 or 5 carbon atoms. The reaction may also be carried out in two stages, in the latter of which the N-alkyl-#-alkylaminoamide intermediate is converted to the desired product. The reaction is preferably carried out at 150 to 280‹ C. in the presence of a free radical polymerization inhibitor and/or a catalyst such as a metal, an inorganic or organic acid. Examples describe the preparation of N,N-dimethyl-, N,N-diethyl-, N,N-di-n-hexyl-, N,N-di-n-butyl-, and N-isobutylacrylamide.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP782669 | 1969-02-04 | ||
| JP782769 | 1969-02-04 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1268741A true GB1268741A (en) | 1972-03-29 |
Family
ID=26342197
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB460470A Expired GB1268741A (en) | 1969-02-04 | 1970-01-30 | PREPARATION OF N-ALKYL-alpha,beta-UNSATURATED AMIDE |
Country Status (3)
| Country | Link |
|---|---|
| FR (1) | FR2046122A5 (en) |
| GB (1) | GB1268741A (en) |
| NL (1) | NL142151B (en) |
-
1970
- 1970-01-30 GB GB460470A patent/GB1268741A/en not_active Expired
- 1970-01-30 NL NL7001400A patent/NL142151B/en not_active IP Right Cessation
- 1970-02-04 FR FR7003892A patent/FR2046122A5/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| DE2005082B2 (en) | 1976-05-26 |
| NL7001400A (en) | 1970-08-06 |
| NL142151B (en) | 1974-05-15 |
| DE2005082A1 (en) | 1972-02-17 |
| FR2046122A5 (en) | 1971-03-05 |
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