GB938895A - Improvements in or relating to the purification of aryl secondary phosphine oxides - Google Patents

Improvements in or relating to the purification of aryl secondary phosphine oxides

Info

Publication number
GB938895A
GB938895A GB489361A GB489361A GB938895A GB 938895 A GB938895 A GB 938895A GB 489361 A GB489361 A GB 489361A GB 489361 A GB489361 A GB 489361A GB 938895 A GB938895 A GB 938895A
Authority
GB
United Kingdom
Prior art keywords
phosphine oxide
diaryl
oxide
purification
relating
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
GB489361A
Inventor
James Leonard Willans
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.)
UK Atomic Energy Authority
Original Assignee
UK Atomic Energy Authority
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 UK Atomic Energy Authority filed Critical UK Atomic Energy Authority
Priority to GB489361A priority Critical patent/GB938895A/en
Priority to CH141562A priority patent/CH412886A/en
Priority to DEU8680A priority patent/DE1166777B/en
Publication of GB938895A publication Critical patent/GB938895A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/46Phosphinous acids [R2POH], [R2P(= O)H]: Thiophosphinous acids including[R2PSH]; [R2P(=S)H]; Aminophosphines [R2PNH2]; Derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/025Purification; Separation; Stabilisation; Desodorisation of organo-phosphorus compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/30Phosphinic acids [R2P(=O)(OH)]; Thiophosphinic acids ; [R2P(=X1)(X2H) (X1, X2 are each independently O, S or Se)]
    • C07F9/304Aromatic acids (P-C aromatic linkage)

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Biochemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

Crude diarylphosphine oxides are purified by reacting with a lower (C1-C3 alkyl ketone, isolating the diaryl 2-hydroxy-isoalkyl phosphine oxide so formed, and heating said diaryl 2-hydroxyisoalkyl phosphine oxide in the absence of oxygen and moisture to regenerate the pure diarylphosphine oxide. The diaryl 2-hydroxyisoalkyl phosphine oxide may be purified itself, e.g. by washing or crystallisation. In an example, diphenylphosphine oxide is reacted with acetone to give diphenyl 2-hydroxyisopropyl phosphine oxide. Specifications 938,893 and 938,894 are referred to.
GB489361A 1961-02-09 1961-02-09 Improvements in or relating to the purification of aryl secondary phosphine oxides Expired GB938895A (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
GB489361A GB938895A (en) 1961-02-09 1961-02-09 Improvements in or relating to the purification of aryl secondary phosphine oxides
CH141562A CH412886A (en) 1961-02-09 1962-02-06 Process for the purification of diarylphosphine oxides
DEU8680A DE1166777B (en) 1961-02-09 1962-02-06 Process for the purification of crude diarylphosphine oxides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB489361A GB938895A (en) 1961-02-09 1961-02-09 Improvements in or relating to the purification of aryl secondary phosphine oxides

Publications (1)

Publication Number Publication Date
GB938895A true GB938895A (en) 1963-10-09

Family

ID=9785849

Family Applications (1)

Application Number Title Priority Date Filing Date
GB489361A Expired GB938895A (en) 1961-02-09 1961-02-09 Improvements in or relating to the purification of aryl secondary phosphine oxides

Country Status (3)

Country Link
CH (1) CH412886A (en)
DE (1) DE1166777B (en)
GB (1) GB938895A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114011473A (en) * 2021-11-30 2022-02-08 安徽大学 Non-noble metal copper-based catalyst and application thereof in benzylamine oxidation coupling reaction

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114011473A (en) * 2021-11-30 2022-02-08 安徽大学 Non-noble metal copper-based catalyst and application thereof in benzylamine oxidation coupling reaction
CN114011473B (en) * 2021-11-30 2024-01-30 安徽大学 Non-noble metal copper-based catalyst and application thereof in benzylamine oxidative coupling reaction

Also Published As

Publication number Publication date
DE1166777B (en) 1964-04-02
CH412886A (en) 1966-05-15

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