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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 638559Generated: October 31, 2026

1-(2-Hydroxyethyl)piperazine → HCID 131714478, compound

https://huagongshe.com/reaction/638559

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantMaleic AcidHCID 444266—
ReactantHCID 20252673HCID 20252673—
SolventWaterHCID 962—
SolventDiethyl EtherHCID 3283—
SolventDichloromethane ethylacetateHCID 21226138—
SolventAcetone diethyletherHCID 21584533—
ProductHCID 131714478HCID 13171447855%

Reaction Steps

A solution of 5.7 g of (5-bromomethylisoxazol-3-yl)-4-fluorophenylmethanone in 100 ml of Et2O was added to a solution of 6.5 g of N-beta-hydroxyethylpiperazine in 400 ml of 25% acetone/Et2O. The resulting mixture was stirred at room temperature for 24 hours. This mixture was filtered and the solution was concentrated in vacuo to give an oil. The residue was dissolved in 300 ml of H2O and shortly thereafter a precipitate formed. The solid was filtered and dried to give 5.2 g of crude solid. A solution of 4.3 g of the amine in 50 ml of 50% ethyl acetate/CH2Cl2 was added dropwise to a solution of excess maleic acid in 600 ml of Et2O. The precipitated salt was filtered and recrystallized from 160 ml of isopropanol to yield 5.2 g (55%) of crystals, m.p. 139°-140°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04562187
Source datasetuspto-grants-1985_12
ORD IDord-316db3fcc85c4b198b5e54d65845faa8
Source noteuspto-grants-1985_12