GB734187A - Improvements in the manufacture of organic phosphorus compounds - Google Patents

Improvements in the manufacture of organic phosphorus compounds

Info

Publication number
GB734187A
GB734187A GB1881251A GB1881251A GB734187A GB 734187 A GB734187 A GB 734187A GB 1881251 A GB1881251 A GB 1881251A GB 1881251 A GB1881251 A GB 1881251A GB 734187 A GB734187 A GB 734187A
Authority
GB
United Kingdom
Prior art keywords
alkyl
methyl
phosphorus
chloride
reacting
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
GB1881251A
Inventor
Harold Coates
Philip Rufus Carter
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.)
Minister of Supply In Her Majesty S Government
Original Assignee
Minister of Supply In Her Majesty S Government
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 Minister of Supply In Her Majesty S Government filed Critical Minister of Supply In Her Majesty S Government
Priority to GB1881251A priority Critical patent/GB734187A/en
Publication of GB734187A publication Critical patent/GB734187A/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 System
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/38Phosphonic acids RP(=O)(OH)2; Thiophosphonic acids, i.e. RP(=X)(XH)2 (X = S, Se)
    • 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 System
    • C07F9/02Phosphorus compounds
    • C07F9/28Phosphorus compounds with one or more P—C bonds
    • C07F9/535Organo-phosphoranes

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  • 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)

Abstract

Alkyl phosphorus tetrafluorides are obtained by reacting a complex compound derived from an alkyl chloride, phosphorus trichloride and anhydrous aluminium trichloride with hydrogen fluoride. The alkyl phosphorus tetrafluoride may be converted into an alkyl phosphonyl compound by the introduction of oxygen, e.g. by reacting with sulphur dioxide to produce an alkyl phosphonyl difluoride, or by reacting with water to produce an alkyl phosphonic acid. Specified alkyl groups are methyl and ethyl. In an example a mild steel autoclave is charged with (CH3.PCl3.AlCl4) complex and anhydrous hydrogen fluoride, the latter being contained in a suspended polythene bucket. The reactants are then mixed and allowed to stand at room temperature for several hours until the autoclave is quite cold. The gaseous contents of the autoclave comprising essentially methyl phosphorus tetrafluoride (CH3.PF4), hydrogen chloride, and excess hydrogen fluoride are then mixed with a stream of sulphur dioxide and the mixed gases passed through an iron tube containing stainless steel gauze and kept at 100 DEG C. The off-gases are condensed in a copper pipe kept at about -75 DEG C. to yield methyl phosphonyl difluoride (CH3POF2), the identity of which is checked by hydrolysing a sample with dilute hydrochloric acid to form methyl phosphonic acid. The complex compound derived from methyl chloride can be produced in known manner by combining the three components in equimolecular proportions in an additive reaction. The Provisional Specification refers to the use of a complex of an alkyl halide, phosphorus trichloride and aluminium chloride.
GB1881251A 1951-08-09 1951-08-09 Improvements in the manufacture of organic phosphorus compounds Expired GB734187A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB1881251A GB734187A (en) 1951-08-09 1951-08-09 Improvements in the manufacture of organic phosphorus compounds

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB1881251A GB734187A (en) 1951-08-09 1951-08-09 Improvements in the manufacture of organic phosphorus compounds

Publications (1)

Publication Number Publication Date
GB734187A true GB734187A (en) 1955-07-27

Family

ID=10118831

Family Applications (1)

Application Number Title Priority Date Filing Date
GB1881251A Expired GB734187A (en) 1951-08-09 1951-08-09 Improvements in the manufacture of organic phosphorus compounds

Country Status (1)

Country Link
GB (1) GB734187A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2904588A (en) * 1956-03-26 1959-09-15 Du Pont Fluorophosphoranes and their preparation
WO2005049628A1 (en) * 2003-11-17 2005-06-02 Merck Patent Gmbh Method for the production of mono(fluoroalkyl)phosphoranes, bis(fluoroalkyl)phosphoranes, and the corresponding acids and phosphates

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2904588A (en) * 1956-03-26 1959-09-15 Du Pont Fluorophosphoranes and their preparation
WO2005049628A1 (en) * 2003-11-17 2005-06-02 Merck Patent Gmbh Method for the production of mono(fluoroalkyl)phosphoranes, bis(fluoroalkyl)phosphoranes, and the corresponding acids and phosphates
US7541488B2 (en) 2003-11-17 2009-06-02 Merck Patent Gmbh Process for the preparation of mono- and bis(fluoroalkyl)phosphoranes and the corresponding acids and phosphates

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