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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1941630Generated: November 2, 2026

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

https://huagongshe.com/reaction/1941630

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-hydroxy-benzyl)-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 numberUS05703096
Source datasetuspto-grants-1997_12
ORD IDord-b7ed13fea3d14bcb9d96597d5518110a
Source noteuspto-grants-1997_12