GB750222A - Improvements in the production of amides - Google Patents

Improvements in the production of amides

Info

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
Application number
GB2406852A
Inventor
Irene Marianne Cohn
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.)
Acordis UK Ltd
Original Assignee
British Celanese Ltd
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.)
Filing date
Publication date
Application filed by British Celanese Ltd filed Critical British Celanese Ltd
Priority to GB2406852A priority Critical patent/GB750222A/en
Publication of GB750222A publication Critical patent/GB750222A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D201/00Preparation, separation, purification or stabilisation of unsubstituted lactams
    • C07D201/16Separation 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.
GB2406852A 1952-09-25 1952-09-25 Improvements in the production of amides Expired GB750222A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (2)

* Cited by examiner, † Cited by third party
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
US2964535A (en) Purification of nu-methyl pyrrolidone
GB750222A (en) Improvements in the production of amides
ES402473A1 (en) Process for removing lactams
GB1106740A (en) Process for the preparation of lactams
US2737511A (en) Extraction of lactam
GB1083085A (en) Process for the recovery of free sulfuric acid from ammonium bisulfate
GB1123732A (en) Preparation of ªÏ-laurinolactam
US3609142A (en) Beckmann rearrangement of cyclic ketoximes to lactams
GB1462740A (en) Process for the recovery of epsilon-caprolactam from reaction mixture of epsilon-caprolactam and sulphuric acid
GB1090044A (en) Preparation of lactams from cyclo-aliphatic ketoximes
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
US2744107A (en) Method for the preparation of lactams
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
NO115580B (en)
GB852130A (en) Separation of organic bases
US3484434A (en) Separation of lactams and cycloalkanone oximes
GB1286427A (en) Process of purifying lactams
Bremner et al. Transformations of penicillins: reactions of penam S-oxides with N-chloro-N-sodiocarbamates