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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112731Generated: November 3, 2026

1-Phenylpiperazine → 1-(4-Phenyl-2-thiazolylmethyl)-4-phenylpiperazine

https://huagongshe.com/reaction/1112731

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-PhenylpiperazineHCID 7096—
ReactantSodium CarbonateHCID 10340—
Reactant2-(Chloromethyl)-4-phenyl-1,3-thiazoleHCID 22557361—
SolventEthanolHCID 702—
Product1-(4-Phenyl-2-thiazolylmethyl)-4-phenylpiperazineHCID 2276250875%

Reaction Steps

A mixture of crude 2-chloromethyl-4-phenylthiazole (4.19g; 0.02 mole), N-phenylpiperazine (3.24 g; 0.02 mole) and finely-powdered, anhydrous sodium carbonate in absolute ethanol (60 ml) was stirred and boiled under reflux for 8 hours. The solvent was evaporated to dryness, solid residue suspended in water (100 ml) and then extracted with 2 × 100 ml CH2Cl2. The extracts were washed with water and dried over anhydrous MgSO4. On evaporation of the solvent, and recrystallisation of the residue from benzene/60°-80° C. petroleum ether mixture (with charcoal treatment) there was obtained the required product (5.03 g; 75%) having m.p. 142°-3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04123529
Source datasetuspto-grants-1978_10
ORD IDord-163721578a66400cba94f5152a80b4bd
Source noteuspto-grants-1978_10