Back
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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAcetic AnhydrideHCID 7918—
ReactantPotassium CarbonateHCID 11430—
ReactantPiperidin-1-ylmethanolHCID 446909—
SolventEthanolHCID 702—
Product1-[4-(Hydroxymethyl)piperidin-1-yl]ethan-1-oneHCID 18934923—

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04898871
Source datasetuspto-grants-1990_02
ORD IDord-d7b77a4f19934657aad1f55d5fca907b
Source noteuspto-grants-1990_02