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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 277348Generated: October 26, 2026

Methanol → N-[4-(1,3-dioxolyl)phenyl]isatin

https://huagongshe.com/reaction/277348

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantIsatinHCID 7054—
ReactantSodium hydrideHCID 24758—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventChloroformHCID 6212—
SolventDimethylformamideHCID 6228—
ProductN-[4-(1,3-dioxolyl)phenyl]isatinHCID 22016430—

Reaction Steps

Isatin (1.88 g, 0.0128 mol) in anhydrous DMF (100 mL) was cooled in an ice-bath under nitrogen and treated with sodium hydride (0.3 g, 1 equivalent). The reaction was warmed to room temperature and stirred for 1 hour. It was then treated with 2-(4-bromophenyl)-1,3-dioxalane (2.83 g, 0.0124 mol) followed by CuI (4.71 g, 2 equivalents). This suspension was heated in an oil-bath at 135° C. under nitrogen for 16 hours. It was then cooled to room temperature and diluted with an equal volume of chloroform. The resulting suspension was filtered and the filtrate was concentrated under reduced pressure. The residue was suspended in xylenes (100 mL) and evaporated to dryness. A thick, viscous oil was recovered which was used as such for the next reaction. TLC (5% methanol in chloroform) showed clean conversion, Rf (product)=0.91.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06355803B1
Source datasetuspto-grants-2002_03
ORD IDord-c51df4dc831148f48ec79beb81115583
Source noteuspto-grants-2002_03