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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637353Generated: October 27, 2026

Chlorosulfonyl isocyanate → 5-Benzoyl-2-oxindole-1-carboxamide

https://huagongshe.com/reaction/637353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant5-Benzoyl-1,3-dihydro-2H-indol-2-oneHCID 13408164—
SolventTetrahydrofuranHCID 8028—
Product5-Benzoyl-2-oxindole-1-carboxamideHCID 13647643—

Reaction Steps

A mixture of 10.1 g. (42 mmole) of 5-benzoyl-2-oxindole, 4.4 ml. (51 mmole) of chlorosulfonyl isocyanate and 300 ml. of tetrahydrofuran was stirred at room temperature for 6 hours, and then the solvent was removed by evaporation in vacuo. The residue was added to 150 ml. of glacial acetic acid and 300 ml. of water and the resulting mixture was heated under reflux for 2 hours. The reaction mixture was cooled and the supernatant liquid was removed by decantation. The remaining gummy residue was triturated under acetonitrile to give a solid which was recovered by filtration and then recrystallized from a 1:1 mixture of n-propanol and acetonitrile. This gave 4.1 g. of the title compound as a solid, mp. 210°-211° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556672
Source datasetuspto-grants-1985_12
ORD IDord-c80f1609faa74282b2ebda8a321c5ccf
Source noteuspto-grants-1985_12