HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 3-Acetylpyridine
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 29 g/h of methyl nicotinate, 76 g/h of acetic acid and 26 g/h of water was evaporated in an evaporator and passed, together with 10 l/h of nitrogen, at 420° C., over 150 ml of a catalyst which contained 2% by weight of sodium oxide, the remainder being anatase. 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 54%. In addition, pyridine was formed with a selectivity of 41%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04950763 |
| Source dataset | uspto-grants-1990_08 |
| ORD ID | ord-6848b8a3bbf145b9b72eb7545b4891f3 |
| Source note | uspto-grants-1990_08 |