GB956624A - Preparation of tetramethylene sulphone - Google Patents

Preparation of tetramethylene sulphone

Info

Publication number
GB956624A
GB956624A GB4418861A GB4418861A GB956624A GB 956624 A GB956624 A GB 956624A GB 4418861 A GB4418861 A GB 4418861A GB 4418861 A GB4418861 A GB 4418861A GB 956624 A GB956624 A GB 956624A
Authority
GB
United Kingdom
Prior art keywords
preparation
tetramethylene sulphone
ethylene
sulphur dioxide
sulphone
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
GB4418861A
Inventor
Alan John Shipman
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 GB4418861A priority Critical patent/GB956624A/en
Publication of GB956624A publication Critical patent/GB956624A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/46Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings substituted on the ring sulfur atom
    • C07D333/48Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings substituted on the ring sulfur atom by oxygen atoms

Abstract

Tetramethylene sulphone is made by heating at least two moles of ethylene with one mole of sulphur dioxide at super atmospheric pressure. The preferred reaction conditions are 250-350 DEG C., 400-600 atmospheres and ethylene to sulphur dioxide molar ratio between 2 and 10 to 1. An example is provided.
GB4418861A 1961-12-11 1961-12-11 Preparation of tetramethylene sulphone Expired GB956624A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB4418861A GB956624A (en) 1961-12-11 1961-12-11 Preparation of tetramethylene sulphone

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB4418861A GB956624A (en) 1961-12-11 1961-12-11 Preparation of tetramethylene sulphone

Publications (1)

Publication Number Publication Date
GB956624A true GB956624A (en) 1964-04-29

Family

ID=10432180

Family Applications (1)

Application Number Title Priority Date Filing Date
GB4418861A Expired GB956624A (en) 1961-12-11 1961-12-11 Preparation of tetramethylene sulphone

Country Status (1)

Country Link
GB (1) GB956624A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2515064A1 (en) * 1981-10-23 1983-04-29 Centre Nat Rech Scient Rhodium, iridium or cobalt complexes - with substd. phenanthroline or bi:pyridyl ligand, useful as shift conversion catalyst

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2515064A1 (en) * 1981-10-23 1983-04-29 Centre Nat Rech Scient Rhodium, iridium or cobalt complexes - with substd. phenanthroline or bi:pyridyl ligand, useful as shift conversion catalyst

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