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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 506891Generated: November 3, 2026

Formaldehyde → HCID 68465254, compound

https://huagongshe.com/reaction/506891

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
Reactant1-(3-Chlorophenyl)piperazineHCID 1355—
ReactantPropargyl alcoholHCID 7859—
CatalystCupric acetate monohydrateHCID 165397—
SolventChloroformHCID 6212—
ProductHCID 68465254HCID 68465254—

Reaction Steps

1-(3-Chlorophenyl)-piperazine (19.7 g; 0.10 mole) is weighed to propargyl alcohol (11.8 ml; 0.20 mole), copper(II) acetate monohydrate (1.0 g; 5.2 mmoles) is added to it, and 37% aqueous formaline (50 ml) is pipetted to the reaction mixture under stirring. The green suspension is refluxed for 2 hours. Then it is cooled, water and chloroform are added to it and the pale green substance insoluble in both phases are filtered off. The aqueous phase is extracted twice with chloroform, the combined organic phases are dried over sodium sulfate and evaporated. The residual brown oil is dissolved in ethyl acetate, and a solution of 2 molar equivalents of hydrogen chloride in ethyl acetate is dropped to it under stirring. The separated white salt is filtered, digested while hot with isopropanol, cooled and filtered.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786129B2
Source datasetuspto-grants-2010_08
ORD IDord-a45003bb695247d38401ab7f2bc8afc1
Source noteuspto-grants-2010_08