Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Methyl Nicotinate | HCID 7151 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-Acetylpyridine | HCID 9589 | — |
Reaction Steps
A mixture of 22 g/h of methyl nicotinate, 57 g/h of acetic acid and 20 g/h of water was evaporated in an evaporator and passed, together with 10 l/h of nitrogen, at 400° C., over 100 ml of catalyst E, which contained 2% by weight of sodium oxide, the remainder being anatase. The catalyst was prepared similarly to Example 8, by impregnating 980 g of TiO2 carrier I with a solution which contained 20 g of Na2O (as aqueous NaOH). The reaction gases were then cooled and were collected in a receiver. From the discharged two-phase mixture, the organic phase was analyzed by gas chromatography. The conversion of nicotinic ester and of acetic acid was 100% in each case. The selectivity with respect to 3-acetylpyridine was 60%. In addition, pyridine was formed with a selectivity of 29%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04950763 |
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| Source dataset | uspto-grants-1990_08 |
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| ORD ID | ord-7094a2ad2b304387a67469d3c673cb4d |
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| Source note | uspto-grants-1990_08 |
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