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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 370664Generated: October 30, 2026

Allyl bromide → 1-(4-Allyloxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanol

https://huagongshe.com/reaction/370664

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium HydroxideHCID 14797—
Reactant2-(4-Diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)ethanolHCID 3071160—
SolventEthanolHCID 702—
Product1-(4-Allyloxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanolHCID 1032039064%

Reaction Steps

In 1.2 liters of ethanol were dissolved 120 g (0.31 mol) of 2-(4-diphenylmethylpiperazinyl)-1-(4-hydroxyphenyl)-ethanol, 74.8 g (0.62 mol) of allyl bromide and 41 g of potassium hydroxide. The resultant solution was heated with refluxing for one hour. After cooling the solution and then removing the solvent, the residue was added with 1.0 liter of ethyl acetate. The resultant mixture was washed successively with an aqueous 1N solution of sodium hydroxide, water and saturated saline, followed by drying over anhydrous sodium sulfate. The solvent was removed, and the residue was crystallized from a mixed solvent of ethanol and n-hexane to give 84.6 g of 1-(4-allyloxyphenyl)-2-(4-diphenylmethylpiperazinyl)ethanol (yield: 64%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04528194
Source datasetuspto-grants-1985_07
ORD IDord-0aac2fb3855742bda7200f6e4e9e1e46
Source noteuspto-grants-1985_07