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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595501Generated: October 26, 2026

Water → 5-(4-[2-(4-Tert-butyloxycarbonylaminophenyl)ethoxy]benzylidene)thiazolidine-2,4-dione

https://huagongshe.com/reaction/1595501

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidinium acetateHCID 3014295—
Reactanttert-butyl N-{4-[2-(4-formylphenoxy)ethyl]phenyl}carbamateHCID 21704970—
SolventTolueneHCID 1140—
Product5-(4-[2-(4-Tert-butyloxycarbonylaminophenyl)ethoxy]benzylidene)thiazolidine-2,4-dioneHCID 5410055072.6%

Reaction Steps

A solution of 3.41 g (10 mmole) tert-butyl N-{4-[2-(4-formylphenoxy)ethyl]phenyl}carbamate and 1.29 g (11 mmole) 2,4-thiazolidinedione in toluene containing a catalytic amount of piperidinium acetate was refluxed in a Dean-Stark water trap for 3 hours. The reaction was followed by TLC and more 2,4-thiazolidinedione was added during the reaction time. The solution was cooled to room temperature filtered and the precipitate was refluxed in methanol. Another filtration gave 3.2 g (yield 72.6%) 5-(4-[2-(4-tert-butyloxycarbonylaminophenyl)ethoxy]benzylidene)thiazolidine-2,4-dione as a light yellow, solid substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288096B1
Source datasetuspto-grants-2001_09
ORD IDord-d4ad7562dded438cb015b98b0f89d2f4
Source noteuspto-grants-2001_09