GB928412A - Preparation of aryloxysulphur pentafluorides - Google Patents

Preparation of aryloxysulphur pentafluorides

Info

Publication number
GB928412A
GB928412A GB258061A GB258061A GB928412A GB 928412 A GB928412 A GB 928412A GB 258061 A GB258061 A GB 258061A GB 258061 A GB258061 A GB 258061A GB 928412 A GB928412 A GB 928412A
Authority
GB
United Kingdom
Prior art keywords
aryloxysulphur
pentafluorides
pentafluoride
substituted
preparation
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
GB258061A
Inventor
John Reginald Case
Hugh Leithead Roberts
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.)
Imperial Chemical Industries Ltd
Original Assignee
Imperial Chemical Industries 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 Imperial Chemical Industries Ltd filed Critical Imperial Chemical Industries Ltd
Priority to GB258061A priority Critical patent/GB928412A/en
Publication of GB928412A publication Critical patent/GB928412A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C381/00Compounds containing carbon and sulfur and having functional groups not covered by groups C07C301/00 - C07C337/00

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

The invention comprises aryloxysulphur pentafluorides having the general formula ROSF5 wherein R represents the phenyl radical, which may be substituted, for example, by chlorine or bromine atoms. The novel compounds may be made by heating bispentafluorosulphur pentoxide with an aromatic hydrocarbon of the benzene series, which may be substituted, for example benzene, toluene, monochlorobenzene, monobromobenzene and o-xylene. The reaction may be effected in the absence of a solvent or carbon tetrachloride or trichlorofluoromethane may be used to provide a homogeneous reaction medium. The reaction takes place at a temperature between 50 DEG and 250 DEG C., under autogenous pressure. The aryloxysulphur pentafluorides can be nitrated and the nitro groups reduced to amino groups. Examples describe the preparation of phenoxysulphur pentafluoride, p-methylphenoxysulphur pentafluoride and p-chlorophenoxysulphur pentafluoride.
GB258061A 1961-01-23 1961-01-23 Preparation of aryloxysulphur pentafluorides Expired GB928412A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB258061A GB928412A (en) 1961-01-23 1961-01-23 Preparation of aryloxysulphur pentafluorides

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB258061A GB928412A (en) 1961-01-23 1961-01-23 Preparation of aryloxysulphur pentafluorides

Publications (1)

Publication Number Publication Date
GB928412A true GB928412A (en) 1963-06-12

Family

ID=9742079

Family Applications (1)

Application Number Title Priority Date Filing Date
GB258061A Expired GB928412A (en) 1961-01-23 1961-01-23 Preparation of aryloxysulphur pentafluorides

Country Status (1)

Country Link
GB (1) GB928412A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7339081B2 (en) * 2006-07-10 2008-03-04 Air Products And Chemicals, Inc. Route to prepare 4-bromo-1-oxypentafluorosulfanylbenzene

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7339081B2 (en) * 2006-07-10 2008-03-04 Air Products And Chemicals, Inc. Route to prepare 4-bromo-1-oxypentafluorosulfanylbenzene

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