GB673997A - Improvements in or relating to process for making tetraalkyllead compounds - Google Patents
Improvements in or relating to process for making tetraalkyllead compoundsInfo
- Publication number
- GB673997A GB673997A GB26064/49A GB2606449A GB673997A GB 673997 A GB673997 A GB 673997A GB 26064/49 A GB26064/49 A GB 26064/49A GB 2606449 A GB2606449 A GB 2606449A GB 673997 A GB673997 A GB 673997A
- Authority
- GB
- United Kingdom
- Prior art keywords
- magnesium
- alloy
- catalyst
- iodide
- weight
- 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
Links
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01K—ELECTRIC INCANDESCENT LAMPS
- H01K1/00—Details
- H01K1/50—Selection of substances for gas fillings; Specified pressure thereof
-
- 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
Abstract
Tetra-alkyl lead compounds are prepared by reacting an alkylating agent with a sodium-magnesium-lead alloy, preferably in the presence of a catalyst, said alloy containing more than 0.2 atom of magnesium for each atom of lead, said alkylating agent comprising one or more esters of inorganic acids having the desired alkyl group attached to the negative radical, and said catalyst being one or more organic compounds selected from the group comprising ethers, cyclic ethers, tertiary amines and substituted ammonium salts. The alloy may have a composition corresponding to NaaMgbPb, in which the sum of a and b is within the limits of approximately 0.5 and 3, and b is more than 0.2 and less than 3. When a catalyst is employed, the alloy may contain from 5 to 25 per cent by weight of sodium plus magnesium and at least 2.5 per cent by weight of magnesium. When a catalyst is not employed, the alloy may contain from 5 to 20 per cent by weight of sodium plus magnesium and more than 3 per cent by weight of magnesium. The reaction may be conducted at a temperature between 50 DEG and 100 DEG C. for a time between 1\2 and 8 hours or at a temperature between 60 DEG and 85 DEG C. for a time between about 1 to 5 hours. Suitable catalysts mentioned are diethyl, methylethyl, dipropyl, dibutyl and dihexyl ethers, dimethyl ether of ethylene glycol, 1,4-dioxane, anisole, tetraethyl- and trimethylethyl-ammonium iodide, triethyl- and trimethyl-amine and dimethylaniline. Suitable alkylating agents mentioned are the monochloro, -bromo and -iodo derivatives of the paraffin hydrocarbons such as methane, ethane, propane, butane and pentane, and the corresponding trialkylphosphates, e.g. methyl bromide and iodide, ethyl chloride, bromide and iodide, n-propyl chloride, n-butyl bromide, n-amyl chloride and iodide and triethyl phosphate. In the examples, tetraethyl lead is prepared.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US107385A US2535191A (en) | 1949-07-28 | 1949-07-28 | Manufacture of alkyllead compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB673997A true GB673997A (en) | 1952-06-18 |
Family
ID=22316375
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB26064/49A Expired GB673997A (en) | 1949-07-28 | 1949-10-11 | Improvements in or relating to process for making tetraalkyllead compounds |
Country Status (5)
Country | Link |
---|---|
US (1) | US2535191A (en) |
DE (1) | DE875355C (en) |
FR (1) | FR997608A (en) |
GB (1) | GB673997A (en) |
NL (1) | NL71969C (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2960515A (en) * | 1952-11-01 | 1960-11-15 | Sol B Wiczer | Method and composition of preparing lead alkyl compounds |
US3401188A (en) * | 1965-08-05 | 1968-09-10 | Du Pont | Process for making tetramethyl lead |
US3457288A (en) * | 1966-04-13 | 1969-07-22 | Ppg Industries Inc | Process for manufacturing tetraorganolead compounds |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1658544A (en) * | 1923-09-07 | 1928-02-07 | Gen Motors Corp | Process of making lead alkyls |
US1661809A (en) * | 1924-03-25 | 1928-03-06 | Du Pont | Process of making tetra-alkyl lead |
US2000069A (en) * | 1932-05-24 | 1935-05-07 | Du Pont | Preparation of lead alkyls |
-
0
- NL NL71969D patent/NL71969C/xx active
-
1949
- 1949-07-28 US US107385A patent/US2535191A/en not_active Expired - Lifetime
- 1949-10-11 GB GB26064/49A patent/GB673997A/en not_active Expired
- 1949-10-14 FR FR997608D patent/FR997608A/en not_active Expired
- 1949-11-03 DE DEE213A patent/DE875355C/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
US2535191A (en) | 1950-12-26 |
DE875355C (en) | 1953-04-30 |
NL71969C (en) | |
FR997608A (en) | 1952-01-08 |
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