GB609059A - Improvements in or relating to the manufacture of alkyl pyridines - Google Patents
Improvements in or relating to the manufacture of alkyl pyridinesInfo
- Publication number
- GB609059A GB609059A GB6775/46A GB677546A GB609059A GB 609059 A GB609059 A GB 609059A GB 6775/46 A GB6775/46 A GB 6775/46A GB 677546 A GB677546 A GB 677546A GB 609059 A GB609059 A GB 609059A
- Authority
- GB
- United Kingdom
- Prior art keywords
- per cent
- alkyl
- alumina
- silica gel
- pyridines
- 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
Landscapes
- Pyridine Compounds (AREA)
- Catalysts (AREA)
Abstract
Alkyl pyridines are produced by passing a vaporized aliphatic carbonyl compound of the formula R-CO-R1, where R is an alkyl or alkenyl group and R1 is hydrogen, alkyl or alkenyl, in admixture with a molal excess of ammonia, at a suitable conversion temperature, over a synthetic silica gel catalyst promoted with a minor proportion of alumina. Acetaldehyde or paraldehyde yields 2- and 4-methyl pyridines. Inert diluents such as methane, ethane or nitrogen may be present. Other carbonyl compounds specified are propionaldehyde, butyraldehyde, valeraldehyde, crotonic and tiglic aldehydes, acetone and methyl ethyl ketone. Suitable catalysts are prepared as described in U.S.A. Specifications 2,142,324 and 2,147,985. A hydrous silica gel is prepared from alkali silicate and acid, treated with an aluminium salt solution, washed and dried. The hydrous alumina which is adsorbed by the silica is generally not in excess of 10 per cent, usually 0.1-2 per cent by weight of the catalyst. Reaction conditions are generally within the ranges 500-1200 DEG F., pressure from atmospheric to 500 p.s.i., and contact time 0.1-5 secs. In examples, acetaldehyde and ammonia in 1 : 3 molar ratio are passed with nitrogen over a synthetic gel containing 1.5 per cent alumina and 98.5 per cent silica gel at 800-950 DEG F. and atmospheric pressure or 100 p.s.i. to yield 2- and 4-methyl pyridines and homologues.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US609059XA | 1944-12-11 | 1944-12-11 |
Publications (1)
Publication Number | Publication Date |
---|---|
GB609059A true GB609059A (en) | 1948-09-24 |
Family
ID=22032471
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB6775/46A Expired GB609059A (en) | 1944-12-11 | 1946-03-05 | Improvements in or relating to the manufacture of alkyl pyridines |
Country Status (1)
Country | Link |
---|---|
GB (1) | GB609059A (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2830974A (en) * | 1955-09-12 | 1958-04-15 | Phillips Petroleum Co | Recovery of unreacted vinylpyridine monomer from polymerization systems |
US2830975A (en) * | 1955-10-17 | 1958-04-15 | Phillips Petroleum Co | Copolymerization of a vinylpyridine and a conjugated diene |
DE1210858B (en) * | 1957-03-26 | 1966-02-17 | Robert S Aries | Process for producing 2, 4, 6-trimethylpyridine |
-
1946
- 1946-03-05 GB GB6775/46A patent/GB609059A/en not_active Expired
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2830974A (en) * | 1955-09-12 | 1958-04-15 | Phillips Petroleum Co | Recovery of unreacted vinylpyridine monomer from polymerization systems |
US2830975A (en) * | 1955-10-17 | 1958-04-15 | Phillips Petroleum Co | Copolymerization of a vinylpyridine and a conjugated diene |
DE1210858B (en) * | 1957-03-26 | 1966-02-17 | Robert S Aries | Process for producing 2, 4, 6-trimethylpyridine |
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