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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863921Generated: October 30, 2026

Ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride → HCID 178517783, compound

https://huagongshe.com/reaction/1863921

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochlorideHCID 2723880—
ReactantSodium ethoxideHCID 2723922—
ReactantTrifluoroacetamidineHCID 2776882—
ReactantSodiumHCID 5360545—
SolventEthanolHCID 702—
ProductHCID 178517783HCID 178517783—

Reaction Steps

To a solution of sodium ethoxide, prepared from 3.2 g (133 mmol) of sodium metal and 200 mL of absolute ethanol, at ambient temperature was added 8.3 g (74 mmol) of trifluoroacetamidine followed by 17.8 g (60 mmol) of ethyl 1-benzyl-3-oxopiperidine-4-carboxylate hydrochloride in portions over 15 min. The reaction mixture was stirred at ambient temperature for 1 h, then heated at reflux for 30 h. The mixture was concentrated in vacuo. The resultant red foam was partitioned between 300 mL of 1N aqueous sodium hydroxide solution and 300 mL of ether. The aqueous layer was washed with 300 mL of diethyl ether and the combined ether phases were extracted with 50 mL of 1N aqueous sodium hydroxide solution. The combined aqueous phases were cooled in an ice-water bath and neutralized to pH 7 with concentration hydrochloric acid. The solids were collected, washed with water, and dried in vacuo to give the title compound as a beige solid, which was used as is in Step B below. An analytical sample was prepared by recrystallization from isopropanol to give the title compound as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07625888B2
Source datasetuspto-grants-2009_12
ORD IDord-ff1666f69772487a83f15ade85656fc3
Source noteuspto-grants-2009_12