GB750222A - Improvements in the production of amides - Google Patents
Improvements in the production of amidesInfo
- Publication number
- GB750222A GB750222A GB2406852A GB2406852A GB750222A GB 750222 A GB750222 A GB 750222A GB 2406852 A GB2406852 A GB 2406852A GB 2406852 A GB2406852 A GB 2406852A GB 750222 A GB750222 A GB 750222A
- Authority
- GB
- United Kingdom
- Prior art keywords
- chloroform
- beckmann
- acetic acid
- water
- extracted
- 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
- C07D201/16—Separation or purification
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Other In-Based Heterocyclic Compounds (AREA)
Abstract
Reaction mixtures containing lactams and un-neutralized mineral acid obtained in the Beckmann transformation of oximes of cyclic ketones, are extracted by means of chloroform to recover the lactam. The Beckmann mixture is preferably diluted with water before extraction so that it contains 100 to 200 grams of sulphuric acid per litre of combined sulphuric acid and water. The extraction may be carried out in the presence of acetic acid or chlorinated acetic acid which may be present in the Beckmann transformation or added to the chloroform. In examples, a Beckmann reaction product containing caprolactam and sulphuric acid is diluted with water and extracted in a column with (1) chloroform, or (2) a mixture of chloroform and acetic acid, (3) and (4) a Beckmann reaction mixture containing acetic acid is diluted with water and extracted with chloroform. The preparation of a lactam from suberone iso-oxime also is referred to. According to the Provisional Specification chloroform may be replaced by other chlorinated aliphatic hydrocarbons, e.g. methylene chloride, trichlorethane, tetrachlorethane, trichlorethylene and perchlorethylene. Specifications 740,891 and 750,221 are referred to.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2406852A GB750222A (en) | 1952-09-25 | 1952-09-25 | Improvements in the production of amides |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB2406852A GB750222A (en) | 1952-09-25 | 1952-09-25 | Improvements in the production of amides |
Publications (1)
Publication Number | Publication Date |
---|---|
GB750222A true GB750222A (en) | 1956-06-13 |
Family
ID=10205852
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB2406852A Expired GB750222A (en) | 1952-09-25 | 1952-09-25 | Improvements in the production of amides |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB750222A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4021422A (en) * | 1974-08-05 | 1977-05-03 | Stamicarbon B.V. | Process for the recovery of ε-caprolactam from reaction mixture of ε-caprolactam and sulphuric acid |
EP0002300A1 (en) * | 1977-12-02 | 1979-06-13 | Stamicarbon B.V. | Process for the recovery of 2-pyrrolidone |
-
1952
- 1952-09-25 GB GB2406852A patent/GB750222A/en not_active Expired
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4021422A (en) * | 1974-08-05 | 1977-05-03 | Stamicarbon B.V. | Process for the recovery of ε-caprolactam from reaction mixture of ε-caprolactam and sulphuric acid |
EP0002300A1 (en) * | 1977-12-02 | 1979-06-13 | Stamicarbon B.V. | Process for the recovery of 2-pyrrolidone |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
GB1088812A (en) | Continuous production of laurolactam in the liquid phase | |
GB750222A (en) | Improvements in the production of amides | |
SU656513A3 (en) | Method of isolating e-caprone lactam | |
US4239682A (en) | Purification of caprolactam | |
GB1397289A (en) | Process for the recovery of lactam | |
US2737511A (en) | Extraction of lactam | |
GB1123732A (en) | Preparation of ªÏ-laurinolactam | |
US3609142A (en) | Beckmann rearrangement of cyclic ketoximes to lactams | |
GB736196A (en) | Improvements relating to the recovery of lactams from reaction products obtained by a beckmann transformation of cyclic ketoximes | |
GB1462740A (en) | Process for the recovery of epsilon-caprolactam from reaction mixture of epsilon-caprolactam and sulphuric acid | |
GB1137037A (en) | Process for the extraction and the concentration of hydrogen fluoride | |
GB1090044A (en) | Preparation of lactams from cyclo-aliphatic ketoximes | |
GB1088033A (en) | Preparation of omega-lactams | |
GB1198428A (en) | Solvent Extraction Process for Caprolactam | |
GB667075A (en) | An improved process for the manufacture of lactams | |
GB995723A (en) | Process for the separation of ªÏ-dodecalactam | |
GB1317638A (en) | Process for the selective production of laurolactam | |
GB1001547A (en) | Process for the separation of ªÏ-dodecalactam | |
GB1353448A (en) | Process for preparing lactams | |
US3364222A (en) | Process for preparing lower alkyl-2-ethylisonicotinic acid esters which are used as intermediates in the preparation of 2-ethylisonicotinic acid thiamide | |
GB873257A (en) | Improvements in the production of omega-aminododecane acidlactam, and a new intermediate compound therein | |
US3700669A (en) | Separation and purification process for lactams | |
GB852130A (en) | Separation of organic bases | |
GB1286427A (en) | Process of purifying lactams | |
Bremner et al. | Transformations of penicillins: reactions of penam S-oxides with N-chloro-N-sodiocarbamates |