GB839172A - Preparation of organic lead compounds - Google Patents
Preparation of organic lead compoundsInfo
- Publication number
- GB839172A GB839172A GB24186/58A GB2418658A GB839172A GB 839172 A GB839172 A GB 839172A GB 24186/58 A GB24186/58 A GB 24186/58A GB 2418658 A GB2418658 A GB 2418658A GB 839172 A GB839172 A GB 839172A
- Authority
- GB
- United Kingdom
- Prior art keywords
- lead
- july
- diethyl ether
- organic solvent
- aryl
- 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
-
- C—CHEMISTRY; METALLURGY
- C25—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES; APPARATUS THEREFOR
- C25B—ELECTROLYTIC OR ELECTROPHORETIC PROCESSES FOR THE PRODUCTION OF COMPOUNDS OR NON-METALS; APPARATUS THEREFOR
- C25B3/00—Electrolytic production of organic compounds
- C25B3/01—Products
- C25B3/13—Organo-metallic compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Electrochemistry (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Electrolytic Production Of Non-Metals, Compounds, Apparatuses Therefor (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
839,172. Lead organic compounds. NATIONAL ALUMINATE CORPORATION. July 28, 1958 [July 31, 1957], No. 24186/58. Class 41. Lead alkyl or aryl compounds are made by electrolysing a solution of a Grignard reagent dissolved in an organic solvent, using a lead anode which is consumed during the process. Diethyl ether or its homologues or tetra hydrofuran may be used as organic solvent, in which the lead alkyl or aryl produced is soluble and is separated by distillation. Polyoxyalkylene ethers may also be used as solvents when the lead compound forms a separate layer. In examples, ethyl magnesium bromide is dissolved in diethyl ether, and the electrodes are well separated, or the cathode of platinum is provided with spacers. The temperature of electrolysis is about the boiling point of the solvent and a reflux condenser is provided; alternatively the process is conducted under pressure.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US675260A US3007857A (en) | 1957-07-31 | 1957-07-31 | Preparation of organic lead compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
GB839172A true GB839172A (en) | 1960-06-29 |
Family
ID=24709710
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB24186/58A Expired GB839172A (en) | 1957-07-31 | 1958-07-28 | Preparation of organic lead compounds |
Country Status (5)
Country | Link |
---|---|
US (1) | US3007857A (en) |
BE (1) | BE569921A (en) |
DE (1) | DE1164406B (en) |
FR (1) | FR1201049A (en) |
GB (1) | GB839172A (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3079311A (en) * | 1961-02-20 | 1963-02-26 | Nalco Chemical Co | Method of preparing tertiary phosphines |
US3100181A (en) * | 1961-02-16 | 1963-08-06 | Nalco Chemical Co | Preparation of organoboranes |
US3234112A (en) * | 1961-03-21 | 1966-02-08 | Nalco Chemical Co | Process of producing organic lead compounds |
US3391066A (en) * | 1959-05-06 | 1968-07-02 | Nalco Chemical Co | Preparation of organic compounds of metals |
US3391067A (en) * | 1959-05-06 | 1968-07-02 | Nalco Chemical Co | Electrolytic process for the preparation of mixed organic lead compounds and electrolyte therefor |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL262356A (en) * | 1960-03-15 | Merck & Co Inc | ||
US3180810A (en) * | 1961-07-31 | 1965-04-27 | Standard Oil Co | Electrolytic cell and method of operation |
US3197392A (en) * | 1961-11-30 | 1965-07-27 | Du Pont | Process for preparing organometal compounds |
DE1226100B (en) * | 1963-09-24 | 1966-10-06 | Halco Chem Co | Process for the production of tetraalkylene lead |
DE1216303B (en) * | 1963-09-24 | 1966-05-12 | Nalco Chemical Co | Electrolyte for the production of lead alkyl compounds |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NL202273A (en) * | 1954-11-26 | |||
BE534128A (en) * | 1954-12-15 | |||
BE540052A (en) * | 1955-06-13 | |||
US2944948A (en) * | 1956-02-06 | 1960-07-12 | Ethyl Corp | Method of purifying organometallic complexes and their use in the preparation of organolead compounds |
-
0
- BE BE569921D patent/BE569921A/xx unknown
-
1957
- 1957-07-31 US US675260A patent/US3007857A/en not_active Expired - Lifetime
-
1958
- 1958-07-28 GB GB24186/58A patent/GB839172A/en not_active Expired
- 1958-07-30 DE DEN15419A patent/DE1164406B/en active Pending
- 1958-07-31 FR FR1201049D patent/FR1201049A/en not_active Expired
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3391066A (en) * | 1959-05-06 | 1968-07-02 | Nalco Chemical Co | Preparation of organic compounds of metals |
US3391067A (en) * | 1959-05-06 | 1968-07-02 | Nalco Chemical Co | Electrolytic process for the preparation of mixed organic lead compounds and electrolyte therefor |
US3100181A (en) * | 1961-02-16 | 1963-08-06 | Nalco Chemical Co | Preparation of organoboranes |
US3079311A (en) * | 1961-02-20 | 1963-02-26 | Nalco Chemical Co | Method of preparing tertiary phosphines |
US3234112A (en) * | 1961-03-21 | 1966-02-08 | Nalco Chemical Co | Process of producing organic lead compounds |
Also Published As
Publication number | Publication date |
---|---|
FR1201049A (en) | 1959-12-28 |
US3007857A (en) | 1961-11-07 |
DE1164406B (en) | 1964-03-05 |
BE569921A (en) |
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