US1045139A - Process of making chlorinated hydrocarbons - Google Patents

Process of making chlorinated hydrocarbons Download PDF

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Publication number
US1045139A
US1045139A US64800011A US1911648000A US1045139A US 1045139 A US1045139 A US 1045139A US 64800011 A US64800011 A US 64800011A US 1911648000 A US1911648000 A US 1911648000A US 1045139 A US1045139 A US 1045139A
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chlorinated hydrocarbons
making
making chlorinated
hydrocarbons
olefinic
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US64800011A
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Otto Graul
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BASF SE
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BASF SE
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C17/00Preparation of halogenated hydrocarbons
    • C07C17/093Preparation of halogenated hydrocarbons by replacement by halogens
    • C07C17/10Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms

Definitions

  • My present invention consistsin a process reaction varies for diflerenthydrocarbons
  • the sulfurous acid which is set free during the reaction remains dissolved in the reaction product andis driven 0H and can be used again for the manufacture of sulfuryl .chlorid.
  • the following example will serve to illustrate further the nature of my invention, which, however, is not confined to this. example.
  • the parts' are by weight. Thoroughly cool about'eighty partsof trimethylethylene (amylene) and add. to it- (slowly and while stirring well) about one hundred and thirty-five parts of cold sulfuryl chlorid, regulating the temperature so that Specification of Letters Patent.

Description

NTTED STTES OTTO GRAUL, OF LUDWIGSHAFEN-ON-THE-RHINE, GERMANY, ASSIGNOR 'IO BADISCHE ANILIN & SODA FABRIK, 0F LUDWIGSHAFEN-ON-THE-RI-IINE, GERMANY, A GOR- IORATION.
PROCESS OF MAKING GHLORINATED HYDROGARBONS.
1,045,139. No Drawing.
To all whom it may concern:
Be it known that I, O'r'ro GRAUL, subject of the Duke of Anhalt, residing at Lud- Wi shafen-on-the-Rhine, Germany, have invented new and useful Improvements in Processes of Making Chlorinated Hydrocarbons, of which the following is a specification.
When olefinic hydrocarbons, such as the olefins themselves C H, are treated with a halogen, there is a difference in the result, as is well known, according to whether chlorin or bromin is used. The reaction with bro- .min results in the smoothproduction of the compounds containing two additional bro-' -min atoms, whereas the addition of chlorin has hitherto always been'accompanied by the formation of considerable quantities of substitution products.
My present invention consistsin a process reaction varies for diflerenthydrocarbons,
but can readily be ascertained. The sulfurous acid which is set free during the reaction remains dissolved in the reaction product andis driven 0H and can be used again for the manufacture of sulfuryl .chlorid.
' The following example will serve to illustrate further the nature of my invention, which, however, is not confined to this. example. The parts' are by weight. Thoroughly cool about'eighty partsof trimethylethylene (amylene) and add. to it- (slowly and while stirring well) about one hundred and thirty-five parts of cold sulfuryl chlorid, regulating the temperature so that Specification of Letters Patent.
I witnesses.
Patented Nov. 26, 1912.
Application filedfieptember 6, 1911. Serial No. 648,000.
tween minus two degrees and zero centigrade. Continue stirring for some time after the addition is effected. Distii off the sulfurous acid and the excess of trimethylethylene and purify the residue, if desired, by distilling in vacuo. The dichlor-pentane thus obtained boils at from forty-eight to fifty-two degrees Centigrade at fortyeight millimeters pressure. This example can, be varied in many respects, for instance if it is desired to produce the dichlorid continuously, the reagents can be separately cooled and run together in a worm in which they gradually assume the temperature at which the reaction takes place. My invention can also be similarly applied to the ghlorination of the other olefinic hydrocarone.
Now what I claim is 1. The process of making chlorinated hydrocarbons by treating olefinic hydrocarbons with sulfuryl chlorid.
2. The process of making chlorinated hydrocarbons by treating an excess of olefinic hydrocarbon with sulfuryl chlorid, distilling oil? the sulfur dioxid and excess of olefinic hydrocarbon and purifying the resulting chlorinated hydrocarbon by distillation.
3. The process of making chlorinated hydrocarbons by treating amylene with sulfuryl chlorid. s
4. The process of making chlorinated hy-v In testimony whereof I have hereunto setmy hand in the presence of two subscribing o '0TT0 GRAUL. Witnesses:
J. ALEC. LLoYD,
J osnrn Fame.
US64800011A 1911-09-06 1911-09-06 Process of making chlorinated hydrocarbons Expired - Lifetime US1045139A (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2549425A (en) * 1947-12-31 1951-04-17 Standard Oil Dev Co Condensation of alkylated naphthalene with a sulfur oxyhalide in presence of friedel-crafts catalyst and mineral oil compositions containing same
US2698348A (en) * 1952-04-02 1954-12-28 Ethyl Corp Halogenation
US2698347A (en) * 1951-01-30 1954-12-28 Ethyl Corp Manufacture of halogen compounds
US3304336A (en) * 1964-05-27 1967-02-14 Detrex Chem Ind Dehydrochlorination of polychlorinated hydrocarbons

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2549425A (en) * 1947-12-31 1951-04-17 Standard Oil Dev Co Condensation of alkylated naphthalene with a sulfur oxyhalide in presence of friedel-crafts catalyst and mineral oil compositions containing same
US2698347A (en) * 1951-01-30 1954-12-28 Ethyl Corp Manufacture of halogen compounds
US2698348A (en) * 1952-04-02 1954-12-28 Ethyl Corp Halogenation
US3304336A (en) * 1964-05-27 1967-02-14 Detrex Chem Ind Dehydrochlorination of polychlorinated hydrocarbons

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