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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1759673Generated: October 30, 2026

Phenothiazine → HCID 22599057, compound

https://huagongshe.com/reaction/1759673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenothiazineHCID 7108—
Reactant1-BromooctaneHCID 8140—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantHCID 22599025HCID 22599025—
SolventDimethylformamideHCID 6228—
ProductHCID 22599057HCID 22599057—

Reaction Steps

A total of 0.2 g of a polymerization inhibitor (phenothiazine) was dissolved in N,N-dimethylformamide. To the resulting solution were added and dissolved 0.62 g (0.0032 mol) of octyl bromide, 2.5 g (0.016 mol) of 1,8-diazabicyclo[5.4.0]-7-undecene (DBU), and 1 g (0.0032 mol) of the above-prepared 1-[4-(9-decenyloxy)phenyl]piperazine, followed by a reaction at 60° C. in an atmosphere of nitrogen gas for 48 hours with stirring. After completion of the reaction, the solution was poured into ice water, extracted with two portions of 300 mL of diethyl ether, washed with 300 mL of distilled water and dehydrated over anhydrous sodium sulfate overnight. After filtration, the solution was diluted with hexane and separated into soluble matters and insoluble matter. The hexane-soluble matter was then recrystallized from ether and hexane (1:3) and thereby yielded the target compound, 1-[4-(9-decenyloxy)phenyl]-4-octylpiperazine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06838129B2
Source datasetuspto-grants-2005_01
ORD IDord-cc9d001da0b345eeb893692fa1a28cef
Source noteuspto-grants-2005_01