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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642038Generated: October 25, 2026

5-Iodoisatin → 4-tert-butyl-N'-(5-iodo-2-oxoindol-3-yl)benzohydrazide

https://huagongshe.com/reaction/642038

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-IodoisatinHCID 88695—
ReactantBenzoic acid, 4-(1,1-dimethylethyl)-, hydrazideHCID 123513—
SolventAcetic AcidHCID 176—
Product4-tert-butyl-N'-(5-iodo-2-oxoindol-3-yl)benzohydrazideHCID 17844097375%

Reaction Conditions

Temperature100 °C

Reaction Steps

Following the general method as outlined in Example 1, into a suspension of 5-iodo-1H-indole-2,3-dione in acetic acid was added 4-tert-butylbenzohydrazide. 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 168 mg of the title compound (75%) as a yellow solid in 99.8% purity by HPLC (Rt: 6.65, gradient of 10 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-fdbfdf3024b4465e97cbdea545049adb
Source noteuspto-grants-2010_04