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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390965Generated: October 31, 2026

1-(2-Methoxyphenyl)piperazine → 3-(4-(2-Methoxyphenyl)piperazin-1-yl)propan-1-ol

https://huagongshe.com/reaction/1390965

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantPotassium CarbonateHCID 11430—
Reactant3-Chloro-1-propanolHCID 12313—
SolventEthanolHCID 702—
SolventDiethyl EtherHCID 3283—
Product3-(4-(2-Methoxyphenyl)piperazin-1-yl)propan-1-olHCID 41090177%

Reaction Conditions

Temperature0 °C

Reaction Steps

46 g of 1-(2-methoxyphenyl)-piperazin and 24.5 g of trimethylene chlorohydrine are dissolved in 200 ml of ethanol, and 25 g of potassium carbonate are added to the solution. The mixture is refluxed for 30 hours, thereafter it is cooled to 0° C, diluted with 50 ml of ethyl ether, filtered, and the filtrate is evaporated. The residue is dissolved in 100 ml of 50° C benzene, the solution is cooled to 0° C, and allowed to stand for 10 hours. The separated crystals are filtered off and dried. 46 g (77%) of 3-[4-(2-methoxyphenyl)-piperazine-1-yl]-1-hydroxy-propane are obtained; m.p.: 92°-93° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04140790
Source datasetuspto-grants-1979_02
ORD IDord-6b88c5bebcd94b5ca76bbe9b378c996a
Source noteuspto-grants-1979_02