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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1709735Generated: October 31, 2026

Acetic Acid → 3-Acetylpyridine

https://huagongshe.com/reaction/1709735

Reaction equation

Participants

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04950763
Source datasetuspto-grants-1990_08
ORD IDord-6848b8a3bbf145b9b72eb7545b4891f3
Source noteuspto-grants-1990_08