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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709736Generated: October 30, 2026

Acetic Acid → 3-Acetylpyridine

https://huagongshe.com/reaction/1709736

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantMethyl NicotinateHCID 7151—
SolventWaterHCID 962—
Product3-AcetylpyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950763
Source datasetuspto-grants-1990_08
ORD IDord-7094a2ad2b304387a67469d3c673cb4d
Source noteuspto-grants-1990_08