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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 637352Generated: October 29, 2026

Toluene → HCID 13647642, compound

https://huagongshe.com/reaction/637352

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTolueneHCID 1140—
ReactantTetrahydrofuranHCID 8028—
ReactantChlorosulfonyl isocyanateHCID 70918—
Reactant6-Phenyl-1,3-dihydro-indol-2-oneHCID 10536384—
SolventWaterHCID 962—
ProductHCID 13647642HCID 13647642—

Reaction Conditions

Temperature5 °C

Reaction Steps

To 4.5 g. (21.5 mmole) of 6-phenyl-2-oxindole in a mixture of 100 ml. of toluene and 25 ml. of tetrahyrofuran was added, with stirring, at 5° C., 2.2 ml. (25.8 mmole) of chlorosulfonyl isocyanate. Stirring was continued for 1 hour at 0°-5° C. and then 100 ml. of water was added. The solid was recovered by filtration and added to a mixture of 40 ml. of glacial acetic acid and 80 ml. of water. The resulting mixture was heated at 100° C. for 1 hour, cooled and filtered. The residue was dried to give 3.1 g. of the title compound, mp. 188°-189° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04556672
Source datasetuspto-grants-1985_12
ORD IDord-7cb2337dad664bcc8a12f121c532d201
Source noteuspto-grants-1985_12