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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814509Generated: November 3, 2026

Tetrahydrofuran → HCID 22503442, compound

https://huagongshe.com/reaction/1814509

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant1-Benzyl-4-piperidoneHCID 19220—
ReactantSodium hydrideHCID 24758—
CatalystPhosphonium, ethyltriphenyl-, bromide (1:1)HCID 73727—
ProductHCID 22503442HCID 2250344252%

Reaction Steps

Ethyl triphenylphosphonium bromide (25 g) was suspended in tetrahydrofuran (100 ml), followed by the addition of 60% sodium hydride (2.68 g) under ice-cooling, and the mixture was stirred at room temperature for 2 hr. The reaction solution was ice-cooled again, followed by the addition of 1-benzyl-4-piperidone (11.55 g), and the resulting mixture was stirred at room temperature overnight. The reaction mixture was partitioned between ethyl acetate and water. The resulting organic layer was washed with water, dried (over MgSO4) and evaporated. The resulting residue was purified by silica gel column chromatography (ethyl acetate/hexane system), to give the title compound as a colorless oil (6.08 g, yield, 52%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875761B2
Source datasetuspto-grants-2005_04
ORD IDord-bbaefd4f88ad4028834431f5dd0b7ea4
Source noteuspto-grants-2005_04