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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1361487Generated: October 30, 2026

1,4-Dioxane hydrochloride → (4-Chloro-phenyl)-[4-(4-hydroxy-pyrrolidin-3-yl)-piperazin-1-yl]-methanone

https://huagongshe.com/reaction/1361487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-Dioxane hydrochlorideHCID 20443148—
Reactant3-[4-(4-Chloro-benzoyl)-piperazin-1-yl]4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl esterHCID 66968681—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
Product(4-Chloro-phenyl)-[4-(4-hydroxy-pyrrolidin-3-yl)-piperazin-1-yl]-methanoneHCID 6696837599%

Reaction Steps

3-[4-(4-Chloro-benzoyl)-piperazin-1-yl]-4-hydroxy-pyrrolidine-1-carboxylic acid tert-butyl ester was dissolved in CH2Cl2. 4M HCl/dioxane (150 mL) was added. The mixture was stirred at RT for 4 h. White precipitate was formed. The mixture was diluted with ether, filtered. The white solid was washed with ether and dried to give desired product (99% yield). 1H-NMR (300 MHz, DMSO, HCl salt): δ 3.0-4.0 (m, 12 H), 4.85 (m, 2 H), 7.25 (d, 2 H), 7.54 (d, 2 H) Retention Time (LC method: formic acid polar): 1.01 min. MS (M+H+): 310

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07880002B2
Source datasetuspto-grants-2011_02
ORD IDord-6ef9d4946ea74227a0fc2bc18c11dde8
Source noteuspto-grants-2011_02