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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1956899Generated: November 2, 2026

Tributylphosphine → 5-{4-[2-(3-Quinolylmethyleneaminooxy)ethoxy]benzyl}-3-tritylthiazolidine-2,4-dione

https://huagongshe.com/reaction/1956899

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTributylphosphineHCID 13831—
Reactant5-(4-Hydroxybenzyl)-3-triphenylmethylthiazolidine-2,4-dioneHCID 2818126—
Reactant2-(3-Quinolylmethyleneaminooxy)ethanolHCID 53749582—
Reactant1,1'-(Azodicarbonyl)dipiperazineHCID 54471820—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product5-{4-[2-(3-Quinolylmethyleneaminooxy)ethoxy]benzyl}-3-tritylthiazolidine-2,4-dioneHCID 7384797992.5%

Reaction Steps

A solution of 0.73 g of 1,1'-(azodicarbonyl)dipiperazine in 10 ml of toluene was added dropwise at room temperature to a suspension of 0.60 g of 2-(3-quinolylmethyleneaminooxy)ethanol (prepared as described in Preparation 3), 1.10 g of 5-(4-hydroxybenzyl)-3-tritylthiazolidine-2,4-dione and 0.72 ml of tributylphosphine in 30 ml of tetrahydrofuran, and the resulting mixture was stirred for 16 hours. At the end of this time, the reaction product was purified by column chromatography through silica gel, using a 1:1 by volume mixture of hexane and ethyl acetate as the eluent, to give 1.45 g of the title compound as a crystalline powder, melting at 127°-130° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05780490
Source datasetuspto-grants-1998_07
ORD IDord-9133d3a2cd2547d382d94b069857f3f6
Source noteuspto-grants-1998_07