GB387924A - Improvements in or relating to the manufacture of dithiocarbamates - Google Patents

Improvements in or relating to the manufacture of dithiocarbamates

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Publication number
GB387924A
GB387924A GB19977/32A GB1997732A GB387924A GB 387924 A GB387924 A GB 387924A GB 19977/32 A GB19977/32 A GB 19977/32A GB 1997732 A GB1997732 A GB 1997732A GB 387924 A GB387924 A GB 387924A
Authority
GB
United Kingdom
Prior art keywords
starting materials
carbon disulphide
gases
carrier gas
reaction
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
GB19977/32A
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.)
Deutsche Hydrierwerke AG
Original Assignee
Deutsche Hydrierwerke AG
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 Deutsche Hydrierwerke AG filed Critical Deutsche Hydrierwerke AG
Publication of GB387924A publication Critical patent/GB387924A/en
Expired legal-status Critical Current

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Abstract

Dithiocarbamates are manufactured by reacting two or more molecular proportions of a primary or secondary amine with one of carbon disulphide, the starting materials being in a gaseous or vaporous state or in a state of very fine subdivision and diluted with a carrier gas which does not react with the starting materials or the reaction product. The process is advantageously carried out by separately vaporizing the carbon disulphide and amine by passing gases through them and then bringing the vapour-laden gases together. According to the vapour pressure of the amine and the dilution desired, larger or smaller quantities of carrier gas are employed. The vaporization may be effected at ordinary, reduced or elevated temperatures according to the vapour pressure of the starting materials. In order to secure a constant output the vaporization is effected in baths of accurately adjusted temperature. Amines which are gaseous at ordinary temperatures are simply mixed with the carrier gas. The process may also be carried out by bringing the starting materials into vapour form by distillation or in the case of difficultly vaporizable amines effecting very fine subdivision by means of atomizing jets, and then diluting with the gases. Suitable carrier gases are nitrogen, hydrogen, carbon monoxide and water gas, also air if care is taken to prevent ignition. The gases after leaving the reaction can be conducted again through the vaporizer. The process may be carried out at ordinary, increased or reduced pressure. If the reaction is too vigorous it can be moderated by cooling. The products, which are precipitated in a very pure, finely pulverulent form and which are of a white colour, are advantageously suited for the rubber industry particularly where colourless or specially coloured kinds of rubber are required. In examples: (1) commercial piperidine and carbon disulphide are vaporized by passing water gas through them and reacted to form piperidine pentamethylenedithiocarbamate; (2) cyclohexylamine and carbon disulphide are vaporized by means of nitrogen and reacted to produce cyclohexylamine cyclohexyldithiocarbamate; (3) dibutylamine (at 80 DEG C.) and carbon disulphide are vaporized by means of hydrogen and reacted to form dibutylamine dibutyldithiocarbamate; (4) dicyclohexylamine is atomized by means of water gas through a nozzle into a reaction chamber where it reacts with a mixture of carbon disulphide and water gas to yield dicyclohexylamine dicyclohexyldithiocarbamate.ALSO:Dithiocarbamates, obtained by reacting two or more molecular proportions of a primary or secondary amine with one of carbon disulphide, the starting materials being in a gaseous or vaporous state or in a state of very fine subdivision and diluted with a carrier gas which does not react with the starting materials or the reaction product, are, on account of their white colour, advantageously suited for the rubber industry, particularly where colourless or specially coloured kinds of rubber are required.
GB19977/32A 1932-06-11 1932-07-14 Improvements in or relating to the manufacture of dithiocarbamates Expired GB387924A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE387924X 1932-06-11

Publications (1)

Publication Number Publication Date
GB387924A true GB387924A (en) 1933-02-16

Family

ID=6371205

Family Applications (1)

Application Number Title Priority Date Filing Date
GB19977/32A Expired GB387924A (en) 1932-06-11 1932-07-14 Improvements in or relating to the manufacture of dithiocarbamates

Country Status (1)

Country Link
GB (1) GB387924A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2561208A (en) * 1948-03-30 1951-07-17 Du Pont Thiocarbamic acid derivatives of alkylenebis
US3210409A (en) * 1960-09-21 1965-10-05 Bayer Ag Process for the continuous production of dithiocarbamates

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2561208A (en) * 1948-03-30 1951-07-17 Du Pont Thiocarbamic acid derivatives of alkylenebis
US3210409A (en) * 1960-09-21 1965-10-05 Bayer Ag Process for the continuous production of dithiocarbamates

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