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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241332Generated: October 26, 2026

1,4-Dioxane → 1-(4-Chlorobenzoyl)piperazine

https://huagongshe.com/reaction/241332

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactanttert-Butyl 4-(4-chlorobenzoyl)piperazine-1-carboxylateHCID 49814251—
SolventDichloromethaneHCID 6344—
Product1-(4-Chlorobenzoyl)piperazineHCID 410148499%

Reaction Steps

4-(4-Chloro-benzoyl)-piperazine-1-carboxylic acid tert-butyl ester (26 g) was dissolved in CH2Cl2 (350 mL). 4M HCL/Dioxane (150 mL) was added. The mixture was stirred at RT for 4 h. White precipitate was formed. The mixture was concentrated. The white solid was washed with Et2O. After the white solid was treated with 1N NaOH (200 mL) and extracted with Ethyl acetate (3×100 mL), the combined organic phase was dried over Na2SO4 and concentrated to give 17.79 g of desired product (99% yield). 1H-NMR (for HCl salt) (300 MHz, MeOD): δ 2.80-2.90 (m, 4H), 3.20-3.80 (m, 4H), 7.29-7.36 (m, 4H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648197B2
Source datasetuspto-grants-2014_02
ORD IDord-97d7bd9150eb4f0f87feb48ae598b1c9
Source noteuspto-grants-2014_02