Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361484Generated: October 25, 2026

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

https://huagongshe.com/reaction/1361484

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, 4 H), 3.20-3.80 (m, 4 H), 7.29-7.36 (m, 4 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880002B2
Source datasetuspto-grants-2011_02
ORD IDord-7f4e8e32b7c6442dbc5d21a19205abd7
Source noteuspto-grants-2011_02