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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266766Generated: October 27, 2026

Allyl chloride → 4-[4-(4-Pyridyl)piperazin-1-yl]phenol allyl ether

https://huagongshe.com/reaction/266766

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl chlorideHCID 7850—
ReactantSodium hydrideHCID 24758—
Reactant4-(4-(4-Pyridyl)piperazin-1-yl)phenolHCID 14986903—
SolventDimethylformamideHCID 6228—
Product4-[4-(4-Pyridyl)piperazin-1-yl]phenol allyl etherHCID 5711579785.7%

Reaction Steps

Sodium hydride (60% dispersion in mineral oil, 0.4 g) was added to a stirred suspension of 4-[4-(4-pyridyl)piperazin-1-yl]phenol (2.55 g) in DMF (25 ml) and the mixture stirred for 20 minutes at room temperature. Allyl chloride (0.756 g) was added dropwise and stirring continued for 20 hours. Ice-water (75 ml) was added and the mixture extracted three times with ethyl acetate. The combined extracts were washed with water and brine, dried (MgSO4) and evaporated. The residue was triturated with hexane and filtered to give 4-[4-(4-pyridyl)piperazin-1-yl]phenol allyl ether (2.5 g) as a solid; NMR(d6DMSO) δ 8.18(2H,dd), 6.8-7.0(6H,m), 5.92-6.13(1H,m), 5.2-5.45(2H,m), 4.5(2H,m), 3.45(4H,m), 3.11(4H,m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652242
Source datasetuspto-grants-1997_07
ORD IDord-85d9ef5ea3d8400c81eb8eb17ac85b53
Source noteuspto-grants-1997_07