HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1199038Generated: November 1, 2026
Water → 1-[4-(Hydroxymethyl)piperidin-1-yl]ethan-1-one
https://huagongshe.com/reaction/1199038
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidin-1-ylmethanol | HCID 446909 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 1-[4-(Hydroxymethyl)piperidin-1-yl]ethan-1-one | HCID 18934923 | — |
Reaction Steps
1-Acetyl-4-hydroxymethylpiperidine may be obtained in the following manner: acetic anhydride (20.5 cc) is added in the course of 15 minutes to a solution of hydroxymethylpiperidine (23.8 g) in ethanol (100 cc) at a temperature in the region of 10° C., and the mixture is stirred for 18 hours at a temperature in the region of 20° C. The reaction mixture is concentrated to dryness under reduced pressure (2.7 kPa); the residue obtained is taken up with water (50 cc) and potassium carbonate (50 g), and the solution is extracted with methylene chloride (3×150 cc); the organic extracts are combined, dried and concentrated to dryness under reduced pressure (2.7 kPa). 1-Acetyl-4-hydroxymethylpiperidine (33.6 g) is thereby obtained in the form of an oil, which is employed in the crude state in the subsequent syntheses.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04898871 |
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| Source dataset | uspto-grants-1990_02 |
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| ORD ID | ord-d7b77a4f19934657aad1f55d5fca907b |
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| Source note | uspto-grants-1990_02 |
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