GB648889A - Improved process for the preparation of amino-carboxylic-acids from lactams - Google Patents
Improved process for the preparation of amino-carboxylic-acids from lactamsInfo
- Publication number
- GB648889A GB648889A GB16942/47A GB1694247A GB648889A GB 648889 A GB648889 A GB 648889A GB 16942/47 A GB16942/47 A GB 16942/47A GB 1694247 A GB1694247 A GB 1694247A GB 648889 A GB648889 A GB 648889A
- Authority
- GB
- United Kingdom
- Prior art keywords
- amino
- acid
- methyl
- preparation
- lactams
- 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
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D201/00—Preparation, separation, purification or stabilisation of unsubstituted lactams
- C07D201/02—Preparation of lactams
- C07D201/08—Preparation of lactams from carboxylic acids or derivatives thereof, e.g. hydroxy carboxylic acids, lactones or nitriles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Abstract
In a preparation of amino-carboxylic acids from aliphatic and cycloaliphatic lactams, the lactam is heated at a temperature between 150 DEG and 300 DEG C. in the presence of more than 20 molecules of water per molecule of lactam. The reaction may be catalysed by the addition of an aliphatic monocarboxylic acid with the general formula CH3(CH2)nCOOH, where n lies between 0 and 20. e -Amino-acid may be obtained by evaporating the solution or concentrating and adding alcohol, acetone, dioxane or a like liquid. In examples: (i) e -Amino-caproic acid (6-amino-hexane-acid) is obtained from caprolactam; (ii) 8-amino-2-methyl-octanoic acid is obtained from methylcyclo - octanone - isoxime. Methyl - cyclooctanone isoxime is prepared by reacting 1-methyl-cyclo-octanone-2 with hydroxylamine and re-arranging the oxime according to Beckmann. Specifications 501,563 and 535,421 are referred to.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
NL648889X | 1946-08-14 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB648889A true GB648889A (en) | 1951-01-17 |
Family
ID=19791999
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB16942/47A Expired GB648889A (en) | 1946-08-14 | 1947-06-26 | Improved process for the preparation of amino-carboxylic-acids from lactams |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB648889A (en) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5391780A (en) * | 1994-04-15 | 1995-02-21 | Eastman Chemical Company | Aqueous process for preparing amido-carboxylic acids by reacting an aminoacid with a carboxylic acid anhydride |
US5393905A (en) * | 1994-04-15 | 1995-02-28 | Eastman Chemical Company | Purification of amido-carboxylic acids |
US5393901A (en) * | 1994-04-15 | 1995-02-28 | Eastman Chemical Company | Aqueous process for preparing amido-carboxylic acids |
US5565590A (en) * | 1994-11-07 | 1996-10-15 | Eastman Chemical Company | Process for recycling amino-carboxylic acid waste materials into amido-carboxylic acids |
-
1947
- 1947-06-26 GB GB16942/47A patent/GB648889A/en not_active Expired
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5391780A (en) * | 1994-04-15 | 1995-02-21 | Eastman Chemical Company | Aqueous process for preparing amido-carboxylic acids by reacting an aminoacid with a carboxylic acid anhydride |
US5393905A (en) * | 1994-04-15 | 1995-02-28 | Eastman Chemical Company | Purification of amido-carboxylic acids |
US5393901A (en) * | 1994-04-15 | 1995-02-28 | Eastman Chemical Company | Aqueous process for preparing amido-carboxylic acids |
US5565590A (en) * | 1994-11-07 | 1996-10-15 | Eastman Chemical Company | Process for recycling amino-carboxylic acid waste materials into amido-carboxylic acids |
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