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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1823933Generated: October 30, 2026

Acetic Acid → HCID 178420113, compound

https://huagongshe.com/reaction/1823933

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantO-XyleneHCID 7237—
ReactantAmmonium AcetateHCID 517165—
Reactant2-(2-Oxo-2-phenyl-ethylcarbamoyl)-piperidine-1-carboxylic acid benzyl esterHCID 23570718—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 178420113HCID 178420113—
ProductHCID 178525127HCID 178525127—

Reaction Conditions

Temperature165 °C

Reaction Steps

2-(2-Oxo-2-phenyl-ethylcarbamoyl)-piperidine-1-carboxylic acid benzyl ester (22.83 g, 60 mmol), NH4OAc (ammonium acetate) (63.5 g, 824 mmol), AcOH (acetic acid) (30 mL), and xylene (350 mL) were mixed at room temperature, and with stirring the reaction mixture was warmed in an oil bath at 165° C. for about 6 hours. The reaction mixture was then cooled to room temperature and poured into brine. The organic phase was dried over MgSO4, filtered, and concentrated under reduced pressure to yield 31.24 g of off white powder. This sample was triturated in ethyl ether (100 mL), filtered, and rinsed liberally with ethyl ether to yield 15.12 g (70% over two steps) of the desired product 2-(4-phenyl-1H-imidazol-2-yl)-piperidine-1-carboxylic acid benzyl ester as a white solid. HPLC analysis showed the compound to be 100% pure at 254 nm and 98.1% pure at 214 nm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07041681B2
Source datasetuspto-grants-2006_05
ORD IDord-7701b4cde6e04fc8a45e1e95d6e1c0ac
Source noteuspto-grants-2006_05