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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 19425Generated: October 27, 2026

Piperidine → HCID 68561168, compound

https://huagongshe.com/reaction/19425

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantEthyl AcetateHCID 8857—
ReactantN,N-diethyl-2-(3-formyl-1H-indol-1-yl)acetamideHCID 820167—
Reactant2,3-dihydro-1H-indolizinium chlorideHCID 68563060—
SolventIsopropanolHCID 3776—
ProductHCID 68561168HCID 68561168—

Reaction Steps

0.800 g of N,N-diethyl-2-(3-formyl-1H-indol-1-yl)acetamide was solubilized in 4.2 ml of isopropanol. 0.238 g of piperidine was added, followed by 0.435 g of 2,3-dihydro-1H-indolizinium chloride dissolved in 7 ml of isopropanol. The reaction mixtures were brought to 80° C. for 24 h, with stirring. 50 ml of ethyl acetate were added in order to precipitate the dye. The precipitate was filtered off, and washed with 3 times with 25 ml of ethyl acetate before being dried under vacuum until a constant weight was obtained. 1.09 g of orange powder were recovered. The analyses were in conformity with the expected structure.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07744658B2
Source datasetuspto-grants-2010_06
ORD IDord-e3890998a6f74fe4bce322bc689e3077
Source noteuspto-grants-2010_06