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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2058942Generated: November 4, 2026

1-(2-Chlorophenyl)piperazine → HCID 20548788, compound

https://huagongshe.com/reaction/2058942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Chlorophenyl)piperazineHCID 415628—
ReactantHCID 20548786HCID 20548786—
SolventEthanolHCID 702—
ProductHCID 20548788HCID 20548788149.8%

Reaction Steps

1,2-Epoxy-3-(2,2-dimethylchroman-4-on-7-yl)oxypropane (7.6 g) and N-(o-chlorophenyl)-piperazine (6.04 g) were heated under reflux in ethanol (150 ml) for 3 hours. The solution was evaporated to dryness in vacuo and treated with an excess of ethanolic hydrogen chloride and evaporated to dryness in vacuo. The residue was crystallised from ethanol/ether to give 1-(4-(o-chlorophenyl)-piperazino)-3-(2,2-dimethylchroman-4-on-7-yl)oxypropan-2-ol hydrochloride (11.07 g), m.p. 169°-173° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04320128
Source datasetuspto-grants-1982_03
ORD IDord-8cd113a0e21e470c94701b6a76b76d46
Source noteuspto-grants-1982_03