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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642037Generated: October 31, 2026

5-Iodoisatin → N'-(5-iodo-2-oxoindol-3-yl)-4-phenoxybenzohydrazide

https://huagongshe.com/reaction/642037

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-IodoisatinHCID 88695—
Reactant4-PhenoxybenzhydrazideHCID 2760339—
SolventAcetic AcidHCID 176—
ProductN'-(5-iodo-2-oxoindol-3-yl)-4-phenoxybenzohydrazideHCID 17851721093%

Reaction Conditions

Temperature100 °C

Reaction Steps

Following the general method as outlined in Example 1, into a suspension of 5-iodo-1H-indole-2,3dione in acetic acid was added 4-phenoxybenzohydrazide. After stirring at 100 ° C., the reaction mixture was cooled to rt and a yellow solid precipitated out. Filtration on a fritté, washing with AcOH, water and drying under vacuo at 60° C. overnight gave 4940 mg of the title compound (93%) as a yellow solid in 99.9% purity by HPLC (Rt: 5.13, gradient of 8 min, MaxPlot detection between 230 and 400 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696231B2
Source datasetuspto-grants-2010_04
ORD IDord-c32473d1d6bb455f91d812226b990886
Source noteuspto-grants-2010_04