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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1007284Generated: October 28, 2026

Benzoic Acid → 5-[4-(4-(2-t-Butoxycarbonylamino-2-methoxycarbonylethyl)phenoxy)benzilidene]thiazolidin-2,4-dione

https://huagongshe.com/reaction/1007284

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
ReactantWaterHCID 962—
ReactantTolueneHCID 1140—
ReactantThiazolidinedioneHCID 5437—
ReactantPiperidineHCID 8082—
ReactantMethyl-2-[(t-butoxycarbonyl)amino]-3-[-(4-formylphenoxy) phenyl]propanoateHCID 22669057—
Product5-[4-(4-(2-t-Butoxycarbonylamino-2-methoxycarbonylethyl)phenoxy)benzilidene]thiazolidin-2,4-dioneHCID 7657311096%

Reaction Steps

To a solution of methyl-2-[(t-butoxycarbonyl)amino]-3-[-(4-formylphenoxy)phenyl]propanoate obtained in step (i) above in anhydrous toluene (10 g, 25 mmol), 2,4-thiazolidinedione (3.53 g, 30 mmol) was added followed by benzoic acid (0.46 g, 3.75 mmol) and piperidine (0.28 g, 3.25 mmol). The solution was heated to reflux at 145-155° C. with continuous removal of water using Dean-Stark apparatus for 5 hr. The solution was cooled to RT and the yellow solid was precipitated to afford the title compound (yield 11.9 g, 96%, purity 96.5% by HPLC, mp: 160-164° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06794401B2
Source datasetuspto-grants-2004_09
ORD IDord-7afe3d99db4f4703bdeb36d3f0dea69f
Source noteuspto-grants-2004_09