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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384841Generated: October 29, 2026

Water → 1-(4-Fluoro-2-methoxyphenyl)piperazine

https://huagongshe.com/reaction/1384841

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBis(2-chloroethyl)amine hydrochlorideHCID 522769—
Reactant4-Fluoro-2-methoxyaniline--hydrogen chloride (1/1)HCID 21183846—
SolventChlorobenzeneHCID 7964—
Product1-(4-Fluoro-2-methoxyphenyl)piperazineHCID 1048865425%

Reaction Conditions

Temperature20 °C

Reaction Steps

9 ml of chlorobenzene and H2O were distilled from a solution of 1.14 g of p-TosOH (6.03×10−3 moles) in 200 ml of chlorobenzene. The solution was cooled to 20° C. and then 1.19 g of 4-fluor-2-methoxyaniline hydrochloride (6.7×10−3 moles) and 1.31 g of bis (2-chloroethyl)amine hydrochloride (7.36×10−3 moles) were added. The reaction was held under reflux for 72 hours after which the solvent was removed and the residue was extracted with 5 ml of NaOH 2N and 30 ml of toluene. The organic phase was washed with H2O, was dried with Na2SO4 and the toluene was removed. The product was purified by silica column using dichloromethane/MeOH (9:1) as mobile phase. An oil was obtained. Yield: 25%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06262056B1
Source datasetuspto-grants-2001_07
ORD IDord-c557cffd5cd54ab384ce3a75a9b6c4f2
Source noteuspto-grants-2001_07