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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156286Generated: November 2, 2026

Acetic Anhydride → 1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanone

https://huagongshe.com/reaction/1156286

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantPotassium CarbonateHCID 11430—
Reactantp-(1-Piperazinyl)phenol dihydrobromideHCID 2723591—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-(4-Hydroxyphenyl)piperazin-1-yl)ethanoneHCID 712441—

Reaction Steps

A mixture of 33.8 parts of 4-(1-piperazinyl)phenol dihydrobromide, 11.2 parts of acetic acid anhydride, 42 parts of potassium carbonate and 300 parts of 1,4-dioxane is stirred and refluxed for 3 days. The reaction mixture is filtered and the filtrate is evaporated. The solid residue is stirred in water and sodium hydrogen carbonate is added. The whole is stirred for 30 minutes. The precipitated product is filtered off and dissolved in a diluted hydrochloric acid solution. The solution is extracted with trichloromethane. The acid aqueous phase is separated and neturalized with ammonium hydroxide. The product is filtered off and crystallized from ethanol, yielding 5.7 parts of 1-acetyl-4-(4-hydroxyphenyl)piperazine; mp. 181.3° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335125
Source datasetuspto-grants-1982_06
ORD IDord-9c81a8e1e5674fdba90baad021030152
Source noteuspto-grants-1982_06