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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1033996Generated: November 2, 2026

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

https://huagongshe.com/reaction/1033996

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-ethoxycarbonyl-phenylacetic 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 ml 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 silica gel (toluene/acetone=10/1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05312924
Source datasetuspto-grants-1994_05
ORD IDord-264abf2b4f1b47388eec894c94b921c5
Source noteuspto-grants-1994_05