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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1110015Generated: November 2, 2026

4-Piperidinecarboxylic acid → 1-Acetylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/1110015

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Piperidinecarboxylic acidHCID 3773—
ReactantAcetic AnhydrideHCID 7918—
Product1-Acetylpiperidine-4-carboxylic acidHCID 117255—

Reaction Steps

100 g of piperidine-4-carboxylic acid were heated under reflux and with stirring at a temperature of 135° C. for 4 hours in 400 ml of acetic anhydride. The mixture was then allowed to cool to room temperature. To work up the reaction mixture it was evaporated to remove acetic anhydride, toluene being added several times towards the end of the evaporation. After the evaporation a beige-colored solid crude product remained as a residue. This was suspended in 300 ml of a mixture of diisopropyl ether and dichloromethane, cooled to a temperature of 0° C. and filtered. 65 g of crude acetylpiperidine-4-carboxylic acid having a melting point of 180° to 182° C. were obtained. The filtrate was diluted while hot with 200 ml of water, and further 1-acetylpiperidine-4-carboxylic acid deposited as a precipitate and was filtered out. 42.91 g of the acid were obtained, so that the total yield of 1-acetylpiperidine-4-carboxylic acid was 107.9 g.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05324725
Source datasetuspto-grants-1994_06
ORD IDord-46907fa7e07a415699c7349e7b5a608e
Source noteuspto-grants-1994_06