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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Piperidinecarboxylic acid | HCID 3773 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Product | 1-Acetylpiperidine-4-carboxylic acid | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05324725 |
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| Source dataset | uspto-grants-1994_06 |
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| ORD ID | ord-46907fa7e07a415699c7349e7b5a608e |
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| Source note | uspto-grants-1994_06 |
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