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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1949073Generated: November 1, 2026

Pyridine → 4-(Acetyloxy)-1-benzylpiperidine-4-carboxylic acid

https://huagongshe.com/reaction/1949073

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantPotassium bisulfateHCID 516920—
Reactant1-Benzyl-4-hydroxypiperidine-4-carboxylic acid hydrochlorideHCID 91844426—
SolventEthanolHCID 702—
SolventDichloromethaneHCID 6344—
Product4-(Acetyloxy)-1-benzylpiperidine-4-carboxylic acidHCID 5330225252%

Reaction Steps

A mixture of 9.4 g 1-benzyl-4-hydroxy-piperidine-4-carboxylic acid, hydrochloride, 3.62 g (35 mmol) acetic anhydride, 11.89 mL pyridine in 40 mL DCM was stirred for 1 h at room temperature. KHSO4 (10%) and ethanol were added and filtered. The filtrate was evaporated and the residue was purified by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile, water and HCOOH. The product containing fractions were evaporated to yield 4.2 g (52%) of the title compound as light yellow solid. MS (m/e): 278.1 [(M+H)+].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399676B2
Source datasetuspto-grants-2013_03
ORD IDord-05f35b198e5c4219b434056fd391e32f
Source noteuspto-grants-2013_03