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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1658644Generated: October 31, 2026

1-(2-Hydroxyethyl)piperazine → HCID 21528501, compound

https://huagongshe.com/reaction/1658644

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-(2-Hydroxyethyl)piperazineHCID 7677—
ReactantHCID 21528388HCID 21528388—
SolventDichloromethaneHCID 6344—
ProductHCID 21528501HCID 21528501—

Reaction Steps

This preparation illustrates methods of preparing cyclic amine derivatives of formula A. In this preparation 1 gram of N-β-hydroxyethyl-piperazine is added to a solution containing 0.31 g. of 5-(3-methanesulfonylprop-1-ynyl)-5H-dibenzo[a,d]cycloheptene, according to Example 3, in 20 ml. of dichloromethane at 0°C. The resulting mixture is monitored by thin-layer chromatographic analysis and allowed to stand at room temperature until conversion of the sulfonate ester is essentially complete. The mixture is then worked up and purified according to the procedure described in Example 4, yielding 5-[3-(N'-β-hydroxyethyl-1-piperazinyl)prop-1-ynyl]-5H-dibenzo[a,d]cycloheptene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03965181
Source datasetuspto-grants-1976_06
ORD IDord-5b412d420d99443683dd69fec94ef25d
Source noteuspto-grants-1976_06