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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637361Generated: October 27, 2026

5-Chlorooxindole → N-isobutyryl-5-chloro-2-oxindole-1-carboxamide

https://huagongshe.com/reaction/637361

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-ChlorooxindoleHCID 152801—
Reactant2-Methylpropanecarbonyl isocyanateHCID 12748637—
SolventTolueneHCID 1140—
ProductN-isobutyryl-5-chloro-2-oxindole-1-carboxamideHCID 1364765223%

Reaction Steps

To a stirred slurry of 8.38 g (0.05 mole) of 5-chloro-2-oxindole in 250 ml of toluene was added 6.79 g (0.06 mole) of isobutyryl isocyanate, and the reaction mixture was heated under reflux for 5.5 hours. The reaction mixture was cooled to room temperature, a small amount of insoluble material was removed by filtration, and then the solvent was removed by evaporation in vacuo. The residue was recrystallized from acetonitrile (with the aid of decolorizing carbon), followed by recrystallization from ethanol, to give 3.23 g of the title compound as pink crystals, m.p. 139°-141° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556672
Source datasetuspto-grants-1985_12
ORD IDord-4141470d1ce646a6b2d9c4e9de47d987
Source noteuspto-grants-1985_12