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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1587071Generated: November 1, 2026

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

https://huagongshe.com/reaction/1587071

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 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 numberUS05216167
Source datasetuspto-grants-1993_06
ORD IDord-ee707f8901c746bf9f6e4756d7829ad0
Source noteuspto-grants-1993_06