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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 567586Generated: October 30, 2026

Carbon Tetrachloride → Ethyl 2-ethoxy-4-[N-(1-(2-piperidino-phenyl)-3-methyl-1-butyl)-aminocarbonylmethyl]benzoate

https://huagongshe.com/reaction/567586

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCarbon TetrachlorideHCID 5943—
ReactantTriethylamineHCID 8471—
ReactantTriphenylphosphineHCID 11776—
Reactant3-Ethoxy-4-ethoxycarbonylphenylacetic acidHCID 10131212—
Reactant3-Methyl-1-(2-piperidino-phenyl)-1-butylamineHCID 10422052—
SolventAcetonitrileHCID 6342—
ProductEthyl 2-ethoxy-4-[N-(1-(2-piperidino-phenyl)-3-methyl-1-butyl)-aminocarbonylmethyl]benzoateHCID 13729227—

Reaction Steps

3 g (11.9 mmols) of 3-ethoxy-4-ethoxycarbonylphenylacetic acid, 3.7 g (14.3 mmols) of triphenylphosphine, 3.3 ml (23.8 mmols) of triethylamine and 1.15 ml (11.9 mmols) of carbon tetrachloride were added successively to a solution of 2.9 g (11.9 mmols) of 3-methyl-1-(2-piperidino-phenyl)-1-butylamine in 29 of acetonitrile. The mixture was then stirred for 15 hours at room temperature, the solvent was removed in vacuo, and the residue was taken up in a mixture of ethyl acetate and water. The organic phase was dried over sodium sulfate, filtered and concentrated by evaporation in vacuo. The evaporation residue was purified by column chromatography on silaca gel (toluene/acetone=10/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE037035E1
Source datasetuspto-grants-2001_01
ORD IDord-cd52593611594f5ba3345129da385455
Source noteuspto-grants-2001_01