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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981411Generated: November 1, 2026

Triethylamine → 1-(2,4-Dibenzyloxyphenylacetyl)-4-benzylpiperidine

https://huagongshe.com/reaction/981411

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-BenzylpiperidineHCID 31738—
ReactantDiethyl cyanophosphonateHCID 76257—
Reactant2-[2,4-Bis(benzyloxy)phenyl]acetic AcidHCID 5028378—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(2,4-Dibenzyloxyphenylacetyl)-4-benzylpiperidineHCID 5446637098.4%

Reaction Steps

To a solution (20 ml) of 4-benzylpiperidine (423 mg) and 2,4-dibenzyloxyphenylacetic acid (700 mg) in N,N-dimethylformamide are added triethylamine (0.56 ml) and diethyl cyanophosphate (393 mg) and the mixture is stirred at room temperature for 15 minutes. Water is added and stirring carried out for 10 minutes, followed by extraction of the product with dichloromethane. The dichloromethane layer is washed with water and dried over anhydrous sodium sulfate. The solvent is distilled off. The residue is subjected to purification by silica gel column chromatography. 1-(2,4-Dibenzyloxyphenylacetyl)-4-benzylpiperidine (1.0 g) in the colorless oily form is obtained from a fraction eluted with dichloromethane-ethyl acetate mixture (8:1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04990511
Source datasetuspto-grants-1991_02
ORD IDord-3d4efafd76cb4adb96b74d8c1ab996f2
Source noteuspto-grants-1991_02