US1749567A - Alkylated lead - Google Patents
Alkylated lead Download PDFInfo
- Publication number
- US1749567A US1749567A US226529A US22652927A US1749567A US 1749567 A US1749567 A US 1749567A US 226529 A US226529 A US 226529A US 22652927 A US22652927 A US 22652927A US 1749567 A US1749567 A US 1749567A
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- Prior art keywords
- lead
- ethyl
- sodium
- reaction
- chloride
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
- C07F7/24—Lead compounds
Definitions
- This invention relates to the preparation of alkylated lead and more particularly to the production of such a compound at substantially atmospheric pressure.
- the ethyl bromide process recently developed, and disclosed in British Patent 216,083 of 1925, includes as its essential feature the progressive addition of water over long periods of time to a mixture of ethyl bromide and alloy.
- the temperature maintained is slightly lower than the boiling temperature of ethyl bromide, and the equipment for carrying out the reaction includes a reflux condenser.
- the reaction also requires the presence of a catalyst, such as pyridine or dimethyl-aniline.
- An object of my invention is to induce the reaction between alkyl chloride and leadsodium alloy under such conditions that neither the use of water and tertiary amine, nor the use of pressure should be necessary.
- a further object of my invention is to eliminate the excess temperature sometimes obtainable, particularly with the process disclosed in British Patent 214,221, with resulting losses in yield of tetra ethyl lead.
- the conducting of the reaction under a reflux condenser has a very decided advantage, that of cooling even the interior portions .of the reacting mass.
- the heat required by the vaporization is withdrawn from any portion of the charge where contact with ethyl chloride is maintained, and where the temperature has been raised to the boiling point of the liquid.
- this heat is permanently removed from the system.
- the tetra ethyl lead may be removed. from the completed reaction mass by steam distillation, or by extraction with a suitable sol-' vent.
- the ethyl chloride may be mixed with an inert solvent, such as benzene, toluene, gasoline and kerosene.
- an inert solvent such as benzene, toluene, gasoline and kerosene.
- Such mixtures have higher boiling temperatures than has ethyl chloride and they, therefore, allow the use of higher temperatures than the boiling point of pure ethyl chloride.
- the alloy used in this work contained 10% sodium and 90% lead, excepting where the sodium was replaced in small amounts by its equivalent 0 potassium.
- Example brine cooled condenser add 50 parts of ethyl chloride and 100 parts of sodium-potassiumlead alloy containing 9.1% sodium and 1.5% potassium. Reflux at the boiling temperature for six hours. Drown the charge in 300 parts of water and distill off the tetra ethyl .lead with steam.
- Example D agitate a mixture 1 of 20 parts of toluene, 50 parts of ethyl chloride, and parts of an alloy containing 10% sodium and 90% lead for 20 hours;
- Example E In a vessel agitate a mixture of 50 parts kerosene, 20 parts of ethyl chloride and 65 parts of an alloy containing 9.4% sodium, 0.8% potassium and 89.8% lead for twelve hours, maintaining a temperature of 21-23 C. for the entire eriod. Extract the tetra ethyl lead from t e finished reaction mass with gasoline.
- a process for making an alkylated lead which comprises efiecting a reaction solely between an alloy of lead with at least one alkali metal, and an alkyl chloride, at substantially atmospheric pressure.
- a process for making an alkylated lead which comprises effecting a reaction between an alloy of lead with a mixture of alkali metals, and an alkyl chloride, at substantially atmospheric pressure.
- a process for making a compound PbR in which R is an alkyl group containing from two to four carbon atoms which comprises effecting a reaction solely between an alloy of lead with at least one alkali metal, and an alk l chloride containing not more than four car on atoms, at substantially atmospheric pressure.
- a rocess for making a compound PbR in whic R is an alkyl group containing from two to four carbon atoms, which com rises eifecting a reaction between an alloy 0 lead with a mixture of sodiumand potassium, and an alkyl chloride containing not more than of lead with at least one alkali metal, and an alkyl chloride containing not more than four carbon atoms, at substantially atmospheric pressure, and in the presence of a diluent.
- a process for making a compound PbR in which R is an alkyl group containing from two to four carbon atoms which comprises effecting a reaction between an alloy of lead, sodium, and potassium, and an alkyl chloride containing not more than four atoms, at substantially atmospheric pressure, the ratio of lead to sodium in the alloy being approximately 10 1 and the ratios of sodium to poztassium being between the limits 20: 1 and :1.
- a process for making tetra ethyl lead which comprises effecting a reaction between an alloy of lead, sodium, and potassium, and ethyl chloride, at substantially atmospheric pressure, the ratio of lead to sodium in the alloy being approximately 10:1 and the ratio of sodium to potassium being between the limits 20 1 and 7:1.
- a process for making lead tetra ethyl which comprises effecting a reaction between ethyl chloride and an alloy of lead, sodium, an potassium, at substantially atmospheric pressure.
- a process for making lead tetra ethyl which comprises eflectin a reaction between eth '1 chloride and an al 0y of lead, sodium, an potassium, at substantially atmospheric pressure, and at the boiling temperature of the reaction mixture, condensing the vaporized ethyl chloride and returning it to the reaction vessel.
- a rocess for making a compound PbR in whic R is an alkyl group containing from two to fourcarbon atoms, which comprises efiecting a reaction solely between an alloy of lead with at least one
Description
Patented Mar. 4, 1930 UNITED STATES PATENT OFFICE HERBERT W. DAUDT, OF OARNEYS POINT, NEW JERSEY, ASSIGNOR TO E. I. DU PON'I.
DE NEMOURS & COMPANY, OF WILMINGTON, DELAWARE, A CORPORATION OF DELA- WARE ALKYLA'IED LEAD 1T0 Drawing.
This invention relates to the preparation of alkylated lead and more particularly to the production of such a compound at substantially atmospheric pressure.
The preparation of tetra ethyl lead by the action of alkyl halides on lead-sodium alloys has been accomplished and disclosed in a number in instances. In Ann. d. Chem. 84,308 (1853) J our. Prak. Chem. 60,304 (1853) Lowig disclosed a method for the preparation of tetra ethyl lead by heating alloys of sodium and lead with ethyliodide at the boiling point of the ethyl iodide, a reflux condenser being used to condense and return the ethyl iodide boiled 011?. It was thought that the iodide was essential to this reaction.
According to one authority, Ghira, Gazz. Chim. Ital. 24 (1) 42 (1894), this reaction requires the presence of small amounts of water. More recent developments indicate that the reaction between ethyl bromide and lead-sodium alloys to form tetra ethyl lead will not take place in the absence of water. It is also being shown conclusively in the copending application of K. P. Monroe, Serial No. 701,641, filed March 25, 1924, that water or some other hydroxylic compounds, such as alcohol, must be present in order to induce the desired reaction.
The ethyl bromide process recently developed, and disclosed in British Patent 216,083 of 1925, includes as its essential feature the progressive addition of water over long periods of time to a mixture of ethyl bromide and alloy. The temperature maintained is slightly lower than the boiling temperature of ethyl bromide, and the equipment for carrying out the reaction includes a reflux condenser. The reaction also requires the presence of a catalyst, such as pyridine or dimethyl-aniline.
In the British Patent 214,221 of 1925 to Krauss and Callis, it was found, an entirely different and unexpected condition existed when ethyl bromide or ethyl chloride was heated with lead-sodium alloys under pressure and at temperatures above their normal boiling points, i. e., boiling point under atmospheric pressure conditions. Under these conditions Krauss and Callis found that no Application filed October 15, 1927. Serial No. 226,528.
water or hydroxylic compound is required. Their process, so far as concerns the use of the chloride, has been found to be successfully operative on a large scale. The disclosure of this British patent covers the preparation of not only tetra ethyl lead, but also that tetra alkyl lead compounds in general. However, the process disclosed in this British Patent 214,221 requires the use of pressure and of temperature above the boiling points.
The process of British Patent 214,221 to Krauss and Callis is, however, entirely different from the process of British Patent 216,083 of 1925 to General Motors, the latter requiring the use of water and of tertiary amine as catalysts. In fact, the addition of these two compounds is of decided disadvantage in the Krauss and Callis process. Furthermore, difierent alloys are best suited for these processes. The Krauss and Callis process requires almost a 10% sodium alloy,
(British Patent 214,221) while the General Motors process (British Patent 216,083) uses any alloy containing 15-18% of sodium. In British Patent 214,221 to Krauss and Callis the difliculties inherent in the tendency for the development of excess temperature and pressure wererecognized and were overcome by means of the temperature depending upon the interrupted addition of the alkyl chloride to the alloy contained in an autoclave, as disclosed in U. S. Patent 1,612,131, dated December 28, 1926.
In the co-pending application of Calcott, Parmelee and Lorriman, Serial No. 146,063 filed November 3, 1926, the addition of potassium to the alloy for the purpose of 1ncreasing the yield of tetra ethyl lead has been disclosed.
An object of my invention is to induce the reaction between alkyl chloride and leadsodium alloy under such conditions that neither the use of water and tertiary amine, nor the use of pressure should be necessary. A further object of my invention is to eliminate the excess temperature sometimes obtainable, particularly with the process disclosed in British Patent 214,221, with resulting losses in yield of tetra ethyl lead.
I have succeeded in inducing the reaction ill between ethyl chloride and the allo at the normal boiling temperature (12 C. of theethyl chloride and at even lower temperatures. Thus, I have been able to eliminate the use 'of pressure and of temperatures above the boiling point. I can carry out the reaction in pressureless equipment at the boiling temperature with the use of a reflux condenser to condense and return the ethyl chloride boiled ofl, or, I can conduct it at a temperature below the boiling point of ethyl chloride.
With a pure lead-sodium alloy the reaction at these low temperatures is very slow and only a low yield of tetra ethyl lead is obtained.
But the addition of potassium to the alloy facilitates the reaction to such an extent that excellent yields can be obtained at these low temperatures. The use of 0.7 5%-1.50% potassium in the alloy has enabled me to obtain yields of 7 5-85% of tetra ethyl lead.
The conducting of the reaction under a reflux condenser has a very decided advantage, that of cooling even the interior portions .of the reacting mass. By allowing the ethyl chloride to boil, the heat required by the vaporization is withdrawn from any portion of the charge where contact with ethyl chloride is maintained, and where the temperature has been raised to the boiling point of the liquid. By means of a suitable condensing equipment this heat is permanently removed from the system.
The tetra ethyl lead may be removed. from the completed reaction mass by steam distillation, or by extraction with a suitable sol-' vent.
The ethyl chloride may be mixed with an inert solvent, such as benzene, toluene, gasoline and kerosene. Such mixtures have higher boiling temperatures than has ethyl chloride and they, therefore, allow the use of higher temperatures than the boiling point of pure ethyl chloride.
The alloy used in this work contained 10% sodium and 90% lead, excepting where the sodium was replaced in small amounts by its equivalent 0 potassium.
While I have referred to tetra ethyl lead in particular, in describing my invention, it will be understood that I contemplate using the process in connection withthe preparation of tetra alkyl lead compounds, with the possible exception of tetra methyl lead. In the case of the latter it may be that the reaction would not take place at the normal boiling temperature (23.7C.) of methyl chloride.
In the case of some of the higher alkyl chlorides, their normal boiling temperatures are very likely higher than their reacting temperatures with lead-sodium alloys and so far as is known the prior art does not disclose the ideal conditions for preparing the corresponding invention.
however, affect the preparation of tetra alklyl lead compounds by my new procedure. T followin examples illustrate actual embodiments 0 my invention, but it is te\be understood that these are illustrative only and are not to be taken as in any way limiting my Example A.To a vessel, provided with a brine cooled reflux condenser, add parts of ethyl chloride and 100 arts of sodium lead alloy containing 10% so ium. Reflux at the boiling temperature for 24 hours. Drown the charge in 300 parts of water and distill off the tetra eth 1 lead with steam.
Example brine cooled condenser, add 50 parts of ethyl chloride and 100 parts of sodium-potassiumlead alloy containing 9.1% sodium and 1.5% potassium. Reflux at the boiling temperature for six hours. Drown the charge in 300 parts of water and distill off the tetra ethyl .lead with steam.
.To a vessel, provided with a Example D.In a vessel agitate a mixture 1 of 20 parts of toluene, 50 parts of ethyl chloride, and parts of an alloy containing 10% sodium and 90% lead for 20 hours;
maintaining a temperature of 19-22 G. for
the entire period. Drown the charge in water and distill with steam. After the oil, being distilled, becomes heavier than the water coming over with it, change the receiver and collect the rest of the oil as tetra ethyl lead.
Example E.-In a vessel agitate a mixture of 50 parts kerosene, 20 parts of ethyl chloride and 65 parts of an alloy containing 9.4% sodium, 0.8% potassium and 89.8% lead for twelve hours, maintaining a temperature of 21-23 C. for the entire eriod. Extract the tetra ethyl lead from t e finished reaction mass with gasoline.
Example F.--To a vessel, provided with a reflux condenser, add 90 parts of n-butyl chloride and 100 parts of sodium-potassiumlead alloy containing 9.1% sodium and 1.5% potassium. Reflux at the boiling temperature for 8 hours. Drown the charge in 300 parts of water, add 50 parts of sodium chloride, and distill oil the tetra- (n) butyl lead with steam. Example G.To a vessel, provided with a reflux condenser, add 100 parts of iso-propyl chloride and 100 arts of sodium-potassiumlead alloy containlng 9.1% sodium and 1.5% potassium. Reflux at the boiling temperature for 5 hours. Extract the tetra-iso-propyl lead with benzene.
As many apparently widely difierent embodiments of this invention may be made without departing from the spirit thereof, it is to be understood that I do not intend to limit myself to the specific embodiments thereof except as indicated in the appended claims.
I claim:
1.- A process for making an alkylated lead which comprises efiecting a reaction solely between an alloy of lead with at least one alkali metal, and an alkyl chloride, at substantially atmospheric pressure.
2. A process for making an alkylated lead which comprises effecting a reaction between an alloy of lead with a mixture of alkali metals, and an alkyl chloride, at substantially atmospheric pressure.
3. A process for making a compound PbR in which R is an alkyl group containing from two to four carbon atoms, which comprises effecting a reaction solely between an alloy of lead with at least one alkali metal, and an alk l chloride containing not more than four car on atoms, at substantially atmospheric pressure.
4. A process for making a compound PbR in which R is an alkyl group containing from two to four carbon atoms, which com rises eflecting a reaction between an alloy 0 lead with a mixture of alkali metals, and an alkyl chloride containing not more thanfour carbon atoms, at substantially atmospheric pressure.
5. A rocess for making a compound PbR in whic R is an alkyl group containing from two to four carbon atoms, which com rises eifecting a reaction between an alloy 0 lead with a mixture of sodiumand potassium, and an alkyl chloride containing not more than of lead with at least one alkali metal, and an alkyl chloride containing not more than four carbon atoms, at substantially atmospheric pressure, and in the presence of a diluent.
10. A process for making a compound PbR in which R is an alkyl group containing from two to four carbon atoms, which comprises effecting a reaction between an alloy of lead, sodium, and potassium, and an alkyl chloride containing not more than four atoms, at substantially atmospheric pressure, the ratio of lead to sodium in the alloy being approximately 10 1 and the ratios of sodium to poztassium being between the limits 20: 1 and :1.
11. A process for making tetra ethyl lead,
which comprises effecting a reaction solely between an alloy alkali metal, and ethyl chloride, at substantially atmospheric pressure and in the presence of a diluent.
12. A process for making tetra ethyl lead which comprises effecting a reaction between an alloy of lead, sodium, and potassium, and ethyl chloride, at substantially atmospheric pressure, the ratio of lead to sodium in the alloy being approximately 10:1 and the ratio of sodium to potassium being between the limits 20 1 and 7:1.
13. The process of producing tetra ethyl lead which comprises inducing a reaction between ethyl chloride and a lead-sodium al loy containing potassium at the normal boilin temperature of ethyl chloride.
11 testimony whereo I afiix my si ature. HERB. T W. DA
four carbon atoms, at substantially atmospheric pressure.
6. A process for making lead tetra ethyl which comprises effecting a reaction between ethyl chloride and an alloy of lead, sodium, an potassium, at substantially atmospheric pressure.
7 A process for making lead tetra ethyl which comprises efiectin a reaction between eth l chloride and an a oy of lead, sodium,
an potassium, at substantially atmospheric pressure, and at a temperature a proximat ing the boiling point of ethyl c oride.
8. A process for making lead tetra ethyl which comprises eflectin a reaction between eth '1 chloride and an al 0y of lead, sodium, an potassium, at substantially atmospheric pressure, and at the boiling temperature of the reaction mixture, condensing the vaporized ethyl chloride and returning it to the reaction vessel. Y
9. A rocess for making a compound PbR in whic R is an alkyl group containing from two to fourcarbon atoms, which comprises efiecting a reaction solely between an alloy of lead with at least one
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US226529A US1749567A (en) | 1927-10-15 | 1927-10-15 | Alkylated lead |
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US226529A US1749567A (en) | 1927-10-15 | 1927-10-15 | Alkylated lead |
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US1749567A true US1749567A (en) | 1930-03-04 |
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US226529A Expired - Lifetime US1749567A (en) | 1927-10-15 | 1927-10-15 | Alkylated lead |
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Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2464399A (en) * | 1946-04-10 | 1949-03-15 | Du Pont | Manufacturing tetraethyl lead |
US2464398A (en) * | 1946-03-12 | 1949-03-15 | Du Pont | Manufacturing tetraethyl lead |
US2477465A (en) * | 1946-03-21 | 1949-07-26 | Du Pont | Manufacturing tetraethyl lead |
US2515821A (en) * | 1946-03-29 | 1950-07-18 | Du Pont | Manufacturing tetraethyl lead |
US2635106A (en) * | 1951-10-25 | 1953-04-14 | Ethyl Corp | Process for making tetraethyl lead |
US2982778A (en) * | 1958-02-03 | 1961-05-02 | Ethyl Corp | Manufacture of tetraethyllead |
US3049558A (en) * | 1959-04-29 | 1962-08-14 | Ethyl Corp | Manufacture of tetramethyllead |
-
1927
- 1927-10-15 US US226529A patent/US1749567A/en not_active Expired - Lifetime
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2464398A (en) * | 1946-03-12 | 1949-03-15 | Du Pont | Manufacturing tetraethyl lead |
US2477465A (en) * | 1946-03-21 | 1949-07-26 | Du Pont | Manufacturing tetraethyl lead |
US2515821A (en) * | 1946-03-29 | 1950-07-18 | Du Pont | Manufacturing tetraethyl lead |
US2464399A (en) * | 1946-04-10 | 1949-03-15 | Du Pont | Manufacturing tetraethyl lead |
US2635106A (en) * | 1951-10-25 | 1953-04-14 | Ethyl Corp | Process for making tetraethyl lead |
US2982778A (en) * | 1958-02-03 | 1961-05-02 | Ethyl Corp | Manufacture of tetraethyllead |
US3049558A (en) * | 1959-04-29 | 1962-08-14 | Ethyl Corp | Manufacture of tetramethyllead |
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