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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 975113Generated: October 29, 2026

Tetrahydrofuran → 1-Benzoyl-2-(2-phenylethyl)-2-piperidinecarbonitrile

https://huagongshe.com/reaction/975113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantBenzene, (2-iodoethyl)-HCID 28503—
Reactant1-Benzoyl-2-piperidinecarbonitrileHCID 19028895—
SolventWaterHCID 962—
Product1-Benzoyl-2-(2-phenylethyl)-2-piperidinecarbonitrileHCID 19028850—

Reaction Conditions

Temperature0 °C

Reaction Steps

To 200 ml of tetrahydrofuran containing 140 mmol lithium diisopropylamide was added 15 g of solid 1-benzoyl-2-piperidinecarbonitrile at -78° C. The mixture was stirred for 30 minutes, after which 100 ml of tetrahydrofuran containing 33.2 g of phenethyl iodide was added dropwise at -78° C. After completion of dropwise addition, the temperature of the reaction mixture was gradually increased to 0° C. Then, water was added and the organic layer was separated. The aqueous layer was further extracted with ethyl acetate. The pooled organic layer was dried over anhydrous magnesium sulfate and filtered and the solvent was then distilled off. The residue was purified by silica gel column chromatography using ethyl acetate-hexane (1:2) as the eluent. The solution containing the desired compound was distilled under reduced pressure and the resulting solid was recrystallized from ethyl acetate-hexane to provide 17.3 g of colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05607939
Source datasetuspto-grants-1997_03
ORD IDord-0bfec3304083477fa3deee35b488402d
Source noteuspto-grants-1997_03