GB609059A - Improvements in or relating to the manufacture of alkyl pyridines - Google Patents

Improvements in or relating to the manufacture of alkyl pyridines

Info

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
Application number
GB6775/46A
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Phillips Petroleum Co
Original Assignee
Phillips Petroleum Co
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Phillips Petroleum Co filed Critical Phillips Petroleum Co
Publication of GB609059A publication Critical patent/GB609059A/en
Expired legal-status Critical Current

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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.
GB6775/46A 1944-12-11 1946-03-05 Improvements in or relating to the manufacture of alkyl pyridines Expired GB609059A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (3)

* Cited by examiner, † Cited by third party
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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