Preparation of alkyl carboxylates
AssigneeMobil Oil Corporation
InventorLewis B. Young
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AssigneeMobil Oil Corporation
InventorLewis B. Young
Estimating the term…
A method for preparation of alkyl carboxylate compounds, and especially .alpha.-methylalkyl carboxylate compounds, by reaction of an olefin and a carboxylic acid compound in the presence of a particular type of zeolite catalyst. The zeolites are characterized by a silica to alumina mole ratio of at least 12 and a constraint index of 1 to 12. Zeolites ZSM-5 and ZSM-12 are particularly preferred.
A method for the preparation of an alkyl carboxylate reaction product containing .alpha.-methylalkyl carboxylates as the major alkyl carboxylate product, said method comprising:
Dependencies are inferred from the claim text.
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Preparation of carboxylic acid esters: by reacting carboxylic acids or symmetrical anhydrides onto unsaturated carbon-to-carbon bonds
The rings having more than two atoms in common: the bicyclo ring system containing seven carbon atoms
Acyclic or carbocyclic compounds
Term ended 19 Dec 2000 (estimated)
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1. Field of the Invention
This invention is concerned with a novel method for preparation of alkylcarboxylates, and particularly .alpha.-methylalkyl carboxylates, by reaction of carboxylic acids with olefinic compounds in the presence of a particular type of crystalline zeolite catalyst.
2. Description of the Prior Art
The following examples are provided to illustrate the process of this invention and to aid those in the art in the understanding thereof, but clearly should not be taken as presenting undue limitations thereon:
One gram of HZSM-:12 zeolite (SiO.sub.2 /Al.sub.2 O.sub.3 mole ratio 70) was placed in a 300 cc stainless steel autoclave equipped with a magnetically driven stirrer. The catalyst had been ground to a powder and calcined prior to use. Added 100 ml of a mixture of acetic acid and 1-octene (molar ratio=4/1) and heated to temperature. Samples were withdrawn periodically through a dip tube and analyzed. Results are summarized in TABLE I.
TABLE I ______________________________________ REACTION OF 1-OCTENE AND ACETIC ACID OVER HZSM--12 C.sub.18 H.sub.17 OAc Isomer Reaction Temper- Yield of Distribution Time ature Pressure C.sub.8 OAc 2 3 4 ______________________________________ 3.5 hr 150.degree. C. 160 psig 5.9 wt % 96.9% 2.9% 0.2% 5.6 hr 200.degree. C. 240 psig 23.9 wt % 94.1% 5.5% 0.4% 73.2 hr 200.degree. C. 230 psig 32.2 wt % 91.4% 8.1% 0.5% ______________________________________