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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1605899Generated: October 30, 2026

1-(2-Methoxyphenyl)piperazine → HCID 21545531, compound

https://huagongshe.com/reaction/1605899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
ReactantHCID 22386964HCID 22386964—
SolventEthanolHCID 702—
ProductHCID 21545531HCID 21545531—

Reaction Steps

A solution consisting of 5.0 g. of 1-(2-carbamoylmethylphenoxy)-2,3-epoxypropane and 4.6 g. of 1-(2-methoxyphenyl)piperazine dissolved in 50 ml. of ethanol was allowed to stand at room temperature (~25°C.) for a period of approximately 16 hours. At the end of this time, the resultant precipitate was removed from the reaction mixture by means of suction filtration and subsequently recrystallized from ethyl acetate to give 1-(2-carbamoylmethylphenoxy)-3-[4-(2-methoxyphenyl)piperazin-1-yl]propan-2-ol as the pure free base compound, m.p. 120°-122°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03951983
Source datasetuspto-grants-1976_04
ORD IDord-e93d3aa6e9ca4d6e8e2f7df0349437b0
Source noteuspto-grants-1976_04