US1036224A - Process of making penta- and hexa-chlorethanes. - Google Patents
Process of making penta- and hexa-chlorethanes. Download PDFInfo
- Publication number
- US1036224A US1036224A US67970012A US1912679700A US1036224A US 1036224 A US1036224 A US 1036224A US 67970012 A US67970012 A US 67970012A US 1912679700 A US1912679700 A US 1912679700A US 1036224 A US1036224 A US 1036224A
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- US
- United States
- Prior art keywords
- chlorin
- tetrachlorethane
- hexachlorethane
- penta
- hexa
- 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.)
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/10—Preparation of halogenated hydrocarbons by replacement by halogens of hydrogen atoms
Definitions
- Hexachlorethane has heretofore been tech- I nically produced by Fara-days reaction ,of chlorin on perchlorethylene.
- Tetrachlorethane (acetylenetetrachlorid) has first been used by us to form perchlorethylene, which has heretofore been obtained indirectly from triand penta-chlorethane.
- the Salzbergwerk at Neu-Stassfurt, Germany, (German Patent 174068) reacts with chlorin on a mixture of tetrachlorethane, sulfur chlorid and iron powder, the latter acting as a contact substance.
- the reaction is carried out at a high temperature.
- Thezlight to which the tetrachlorethane-is subjected may be produced by an unenveloped or free arc lamp, a mercury vapor lamp, or other .similar source of artificial light during the admission of the halogen,
- pentachlorethane is then converted into hexachlorethane (perchlorethane) .O HC1 +2Cl:C,Cl -[-I-IC1. It will therefore be seen that penta-chlorethane can be produced by this process.
- the reaction must be stopped at a suitable time, and advantageously as soon as about 10% in excess of the theoretical quantity of halogen has been supplied to the tetrachlorethane.
- the separation of the mixture of about.90% pentachlorethane and 10% hexachlorethane is done by fractional distillation or they may be separated by distilling the hexachlorethane, that has hardcned in the cooler, with steam.
- the process may be carried out continuously by withdrawing a portion of the reaction mass and replacing it with tetrachlorcthane and then cooling that portion which has been removed, whereupon the greater part of the hexachlorethane held in solution will separate; it is then filtered and the filtrate returned to the reaction vessel.
- the hexachlorethane is therefore obtained directly, and pure.
- the process is carried out commercially for instance by placing 300 kilos of tetrachlorethane in a vessel capable of resisting the action of chlorin and containing in its interior a Uviol mercury vapor lamp of suitable length, or any other source of artificial li ht. A rapid stream of chlorin is then a itted, and the rapidly rising temperature is kept down by water cooling to about 60 C.
- the large quantity of hydrochloric acid gas is allowed to pass into a suitable absorber containin water, or into a Riesel tower e. g. of the 'nd of washing towers, scrubbers or the like for absorption or condensation.
- the hydrochloric acid gas, free from water may be led off and directly used for any purpose.
- the present process utilizes the cheap tetrachlorethane obtainable on the market in large quantities as a commercial product and by the use of artificial sources of light it is independent of external conditions, whereLy its technical value in combination with practical simplicity of the process is alone established.
- Patent 204883 states that an excess of chlorin produces tetachlorethane-without any additional products.
- Pentaand hexa-chloret-hane are formed in accordance withour process without danger of explosions or the requirement that the source" of light be kept constant.
- the reaction takes place in the liquid, while the proe esses in the patentsreferred to require the treatment of a gaseous mixture that must be maintained in definite proportions.
- the process of chlorinating tetrachlorethane WhICh comprises reacting on tetrachlorethane with chlorin gas in the presence of light capable of promoting chemical action, the supply of chlorin being sutficient to convert the tetrachlorethane into the higher chlorinated ethane desired to be made.
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
UNITED STATES HERMANE' HABERLAND WALTER SGHAEFER, OF ZSGHERNDORF, GERMANY, AS-
SIGNORS TO THE FIRM 0F SALZBERGWERK NEU-STASSFURT UNI) THEILNEHMER,
OF ZSCHERNDORF, GERMANY.
PROCESS OF MAKING PENTA- AND HEXA-CHLORE'I'HANES.
No Drawing.
certain new and useful Improvements in- Prccesses of Making Pentaand Hexa- Chlorethanes; and we do hereby declare the following to be a full, clear, and exact description of the invention, such as will en- Chem. GentraZbZatt, Berlin 98. I, 883; 11.. '17 5) hexachlorethane results from the enable others skilled in the .art to which it ap-. pertains to make and use the same.
Hexachlorethane has heretofore been tech- I nically produced by Fara-days reaction ,of chlorin on perchlorethylene.
Attempts to commercially manufacture hexachlorethane from a starting material cheaper than perchlorethylene have, up to the present, so far as known by us, not come into use.
Tetrachlorethane (acetylenetetrachlorid) has first been used by us to form perchlorethylene, which has heretofore been obtained indirectly from triand penta-chlorethane. v
Accordin to Mouneyrat (Bulletin S0- cz't Chim: Paris a 19. 182', 4.54; and
ergetic chlorination of tetrachlorethane (acetylene tetrachlorid) by means of alu minium chlorid acting as a chlorin carrier at a temperature of 120 C.
The Salzbergwerk at Neu-Stassfurt, Germany, (German Patent 174068) reacts with chlorin on a mixture of tetrachlorethane, sulfur chlorid and iron powder, the latter acting as a contact substance. The reaction is carried out at a high temperature.
The use of a chlorin carrier, which must be used in large quantities, the comparative slowness of the reaction, the permanent maintenance of elevated temperature, the unavoidable separate purification of the final product, and the working up again of the contact substances have prevented the commercial manufacture, as the costs thereof are prohibitive to the production of a commercial product.
The following process completely avoids all the foregoing difficulties and efiects a direct combination or react-ion that proceeds Specification of Letters Z Patent. Patented Aug. 20, 1912.
Application filed February 24, 1912. Serial No. 679,700.
smoothly and results in a quantitative yield of pure hexachlorethane with the simultaneous production of hydrochloric acid as a by-productthat is free from impurities.
We have discovered that when tetrachlorethane is subjected to the action of chlorin gas in the presence of actinic rays from a source of artificial light it is converted with extraordinary rapidity into hexachlorethane 'without the use of a chlorin carrier or re-.
agent.
Thezlight to which the tetrachlorethane-is subjected may be produced by an unenveloped or free arc lamp, a mercury vapor lamp, or other .similar source of artificial light during the admission of the halogen,
care only being taken to keep the high heat of reaction down, for example, to between 50 and 60 0., by a suitable cooling agent, so as to prevent the products from distilling over, or from sublimation while the hydrochloric acid gas thatis produced in large quantities is condensed or absorbed in a suitable apparatus.
The tetrachlorethane is immediately transformed into pentachlorethane,
and the pentachlorethane is then converted into hexachlorethane (perchlorethane) .O HC1 +2Cl:C,Cl -[-I-IC1. It will therefore be seen that penta-chlorethane can be produced by this process. In
order to do so the reaction must be stopped at a suitable time, and advantageously as soon as about 10% in excess of the theoretical quantity of halogen has been supplied to the tetrachlorethane. The separation of the mixture of about.90% pentachlorethane and 10% hexachlorethane is done by fractional distillation or they may be separated by distilling the hexachlorethane, that has hardcned in the cooler, with steam.
If hexachlorethane is desired, the reaction is carried on until the molecule is saturated with the halogen, namely until the theoretical quantity of chlorin has entered into the reaction and replaced all the hydrogen in the radical, as follows:
c,H,c1;+2c1,=c,c1.+2Hc1. 'After the above-mentioned mixture has been formed the hexachl'orethane begins to separate in time from the mixture and after starting to separate, its formation and precipit-ation is very rapid. As soon as the liquid in the reaction vessel becomes thick and mushy the supply of chlorin is stopped, the white crystals are pressed to squeeze out the adhering liquid, to which .is added a further quantity of tetrachlorethane for the formation of a new quantity of the product.
The process may be carried out continuously by withdrawing a portion of the reaction mass and replacing it with tetrachlorcthane and then cooling that portion which has been removed, whereupon the greater part of the hexachlorethane held in solution will separate; it is then filtered and the filtrate returned to the reaction vessel. The hexachlorethane is therefore obtained directly, and pure.
The process is carried out commercially for instance by placing 300 kilos of tetrachlorethane in a vessel capable of resisting the action of chlorin and containing in its interior a Uviol mercury vapor lamp of suitable length, or any other source of artificial li ht. A rapid stream of chlorin is then a itted, and the rapidly rising temperature is kept down by water cooling to about 60 C. The large quantity of hydrochloric acid gas is allowed to pass into a suitable absorber containin water, or into a Riesel tower e. g. of the 'nd of washing towers, scrubbers or the like for absorption or condensation. The hydrochloric acid gas, free from water may be led off and directly used for any purpose. After su plying 200 kilos of chlorin, at the end 0 about fourteen hours the thick mush of hexachlorethane is formed and the reaction is completed. The pentachlorethane is then pressed out and the crystals are washed with tetrachlorethane. The resulting hexachlorethane is pure white and melts at 183184 C., with simultaneous sublimation. The yield corresponds to the theoretical quantity of chlorin required for the formation of the product, and there is no admixture of by-products.
Faraday observed that hexachlorethane was formed when dichlorethylene and chlorin were subjected to the action of sunlight. The commercial production by such a method is out of the question on account of the great cost of the starting material and the dependence on sunshine.
The present process utilizes the cheap tetrachlorethane obtainable on the market in large quantities as a commercial product and by the use of artificial sources of light it is independent of external conditions, whereLy its technical value in combination with practical simplicity of the process is alone established.
Artificial light has heretofore been only used in producing diand tetra-chloracetylene (German Patents Lidholm 201705 and 204516, and Chemischen Fabrik Griesheim- Elektron, 204883) these processes, however,
give no idea for the furtherchlorination of the products, and Patent 204883 states that an excess of chlorin produces tetachlorethane-without any additional products. The
patents to Lidholm state that the source of light must be constant, or.approximately so, to avoid explosions.
Pentaand hexa-chloret-hane are formed in accordance withour process without danger of explosions or the requirement that the source" of light be kept constant. The reaction takes place in the liquid, while the proe esses in the patentsreferred to require the treatment of a gaseous mixture that must be maintained in definite proportions.
We claim 7 1. The rocess of chlorinating tetrachlorethane which comprises reacting on tetrachlorethane with chlorin gas in the presence of light capable of promoting chemical action. I
2. The process of chlorinating tetrachlorethane WhICh comprises reacting on tetrachlorethane with chlorin gas in the presence of light capable of promoting chemical action, the supply of chlorin being sutficient to convert the tetrachlorethane into the higher chlorinated ethane desired to be made In testimony that we claim the foregoing as our invention, we have signed our names in presence of two subscribing witnesses.
Witnesses RUDOLPH Fmoxn, AUGUST BRZQGER.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US67970012A US1036224A (en) | 1912-02-24 | 1912-02-24 | Process of making penta- and hexa-chlorethanes. |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US67970012A US1036224A (en) | 1912-02-24 | 1912-02-24 | Process of making penta- and hexa-chlorethanes. |
Publications (1)
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US1036224A true US1036224A (en) | 1912-08-20 |
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US67970012A Expired - Lifetime US1036224A (en) | 1912-02-24 | 1912-02-24 | Process of making penta- and hexa-chlorethanes. |
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Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2456173A (en) * | 1945-05-30 | 1948-12-14 | Du Pont | Photochlorination of acetylene |
-
1912
- 1912-02-24 US US67970012A patent/US1036224A/en not_active Expired - Lifetime
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2456173A (en) * | 1945-05-30 | 1948-12-14 | Du Pont | Photochlorination of acetylene |
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