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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212180Generated: October 26, 2026

Acetic Acid → Methyl 3-aminopiperidine-1-carboxylate

https://huagongshe.com/reaction/2212180

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrochloric AcidHCID 313—
Reactant3-(Trityl-amino)-piperidine-1-carboxylic acid methyl esterHCID 69652409—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-aminopiperidine-1-carboxylateHCID 2227309895.6%

Reaction Steps

Add acetic acid saturated with HCl(g) (100 mL, ˜3N in HCl) to 3-(trityl-amino)-piperidine-1-carboxylic acid methyl ester (6.51 g, 16.2 mmol). Stir the solution vigorously at room temperature for 2 hours. Concentrate the reaction, follow this by addition of acetonitrile and concentration to assist in the removal of acetic acid (×2). Partition the resulting material between 1N HCl and ethyl acetate, separate the layers, extract the organic layer with 1N HCl. Basify the combined aqueous layers with 5N sodium hydroxide, extract with 20% isopropanol/chloroform (×3). Dry the combined organic layers over magnesium sulfate and concentrate to give 2.45 g of the title compound as a white solid, 95% yield. 1H NMR: consistent with structure. MS (ion spray) 158 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101891B2
Source datasetuspto-grants-2006_09
ORD IDord-8d411f7d4713493f87e38178998d2b8d
Source noteuspto-grants-2006_09