GB762625A - Improvements in the production of piperazine - Google Patents

Improvements in the production of piperazine

Info

Publication number
GB762625A
GB762625A GB1745454A GB1745454A GB762625A GB 762625 A GB762625 A GB 762625A GB 1745454 A GB1745454 A GB 1745454A GB 1745454 A GB1745454 A GB 1745454A GB 762625 A GB762625 A GB 762625A
Authority
GB
United Kingdom
Prior art keywords
piperazine
production
monoethanolamine
adipate
regenerated
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
GB1745454A
Inventor
Roy James Collins
Valerie Grenville
Vladimir Petrow
Bennett Sturgeon
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.)
BDH Chemicals Ltd
Original Assignee
BDH Chemicals 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 BDH Chemicals Ltd filed Critical BDH Chemicals Ltd
Priority to GB1745454A priority Critical patent/GB762625A/en
Publication of GB762625A publication Critical patent/GB762625A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic 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
    • C07D295/02Heterocyclic 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 containing only hydrogen and carbon atoms in addition to the ring hetero elements
    • C07D295/023Preparation; Separation; Stabilisation; Use of additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Piperazine is manufactured by a process comprising heating monoethanolamine with at least one molar proportion of ammonium chloride or ammonium bromide at a temperature of from approximately 240 DEG to 265 DEG C. Preferably the piperazine is isolated in the form of its adipic acid salt from which it may be regenerated in known manner, e.g. by treating the adipate with concentrated aqueous alkali hydroxide.
GB1745454A 1954-06-14 1954-06-14 Improvements in the production of piperazine Expired GB762625A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1745454A GB762625A (en) 1954-06-14 1954-06-14 Improvements in the production of piperazine

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1745454A GB762625A (en) 1954-06-14 1954-06-14 Improvements in the production of piperazine

Publications (1)

Publication Number Publication Date
GB762625A true GB762625A (en) 1956-11-28

Family

ID=10095460

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1745454A Expired GB762625A (en) 1954-06-14 1954-06-14 Improvements in the production of piperazine

Country Status (1)

Country Link
GB (1) GB762625A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3023211A (en) * 1960-09-12 1962-02-27 Jefferson Chem Co Inc Method for the preparation of piperazine monohydrochloride
US3126383A (en) * 1964-03-24 Method for recovering alkylamine-free

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3126383A (en) * 1964-03-24 Method for recovering alkylamine-free
US3023211A (en) * 1960-09-12 1962-02-27 Jefferson Chem Co Inc Method for the preparation of piperazine monohydrochloride

Similar Documents

Publication Publication Date Title
ES399314A1 (en) Process for the prevention of precipitations in water or aqueous solutions
GB762625A (en) Improvements in the production of piperazine
GB1077036A (en) Process for the production of the sodium salt of 3-hydroxy-2-oxo-1(2h)-pyridine sulphonic acid and the production of 2,3-pyridine diol
GB934292A (en) Process for the preparation of heterocyclic compounds
ES420672A1 (en) Process for the production of di- and polyhydroxycarboxylic acids
GB1078044A (en) A method for producing the meso-form of 2,3-dibromosuccinic acid
GB1039376A (en) Process for preparing bis-hydroxyalkylsulphones and ª‰-hydroxyalkylsulphonic acid salts
GB925506A (en) Process for the production of 2,4,5,6-tetrachloropyrimidine
ES421050A1 (en) Process for recovering ammonium organic salts from aqueous solutions
GB990757A (en) Process for the preparation of 3-acetamido-5-amino-2,4,6,-triiodobenzoic acid
GB772966A (en) Preparation of 2,4,5-trichlorophenoxyacetic acid
GB784070A (en) Process for the production of aliphatic amino-sulphonic acids
ZA706366B (en) Process for the manufacture of salt mixtures of alkali metal salts of o,o-dialkyldithiophosphoric acids
GB939905A (en) A process for preparing a penillic acid and salts thereof
GB829618A (en) Process for producing estrone sulfate salt compounds
GB786561A (en) Manufacture of terephthalic acid
ES351101A1 (en) Process for the manufacture of nitrosyl chloride
GB956605A (en) Penicillanic acid derivatives
GB855504A (en) Preparation of 2-methyl-4-chloro-phenoxy alkanoic acids
GB969439A (en) Process for making hydrazodicarbonamide
GB849000A (en) Polyamide production
GB760099A (en) Production of pyridines
GB1115535A (en) Production of a nitrobenzoic acid
GB823411A (en) Improvements in curing salt compositions
GB732145A (en) Improvements in or relating to a process for preparing pure potassium nitrate commercially free from chlorides and sodium salts