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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11202Generated: October 25, 2026

Methanol → N-[3-(1,3-dioxolyl)phenyl]isatin

https://huagongshe.com/reaction/11202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantIsatinHCID 7054—
ReactantSodium hydrideHCID 24758—
Reactant2-(3-Bromophenyl)-1,3-dioxolaneHCID 87306—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductN-[3-(1,3-dioxolyl)phenyl]isatinHCID 21972258—

Reaction Conditions

Temperature0 °C

Reaction Steps

Isatin (3.2 g, 0.0218 mol) was dissolved in anhydrous DMF (75 ml) and cooled in an ice-bath under a nitrogen atmosphere. To this cold solution, sodium hydride (0.575 g, 0.0239 mol) was added and the reaction was stirred at 0° C. for 1.5 hours. This solution was then treated with 2-(3-bromophenyl)-1,3-dioxolane (5 g, 1 equivalent) followed by CuI (8.3 g, 2 equivalents). The resulting suspension was heated in an oil-bath under nitrogen at 130–140° C. for 16 hours. It was then cooled to room temperature and diluted with an equal volume of chloroform. This suspension was filtered and the filtrate was concentrated under reduced pressure. A viscous brown oil was recovered which was suspended in xylenes (150 ml) wand evaporated to dryness. The residue was used as such for the next reaction. TLC (5% methanol in chloroform) showed clean conversion; Rf (product)=0.86.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07097995B2
Source datasetuspto-grants-2006_08
ORD IDord-0e3a377f9f97467ab5412975fa58ae7c
Source noteuspto-grants-2006_08