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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 365982Generated: October 30, 2026

Allyl bromide → 1-Allyl-3,3-dimethoxyindolin-2-one

https://huagongshe.com/reaction/365982

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantSodium hydrideHCID 24758—
Reactant3,3-Dimethoxy-1,3-dihydro-2H-indol-2-oneHCID 15480745—
SolventDimethylformamideHCID 6228—
Product1-Allyl-3,3-dimethoxyindolin-2-oneHCID 2201311090%

Reaction Steps

A solution of 3.86 g of 3,3-dimethoxyindolin-2-one in 30 ml of N,N-dimethylformamide was added dropwise to a suspension of 1.2 g of sodium hydride (60%) in 40 ml of N,N-dimethylformamide at 0° C. in a nitrogen stream. After the mixture was stirred at that temperature for 30 minutes, 2.60 ml of allyl bromide was added thereto. The resulting mixture was stirred for 1 hour and then concentrated. Chloroform was added to the residue, and the mixture was washed with an aqueous solution of sodium chloride. The organic layer was dried over anhydrous sodium sulfate and concentrated. The resulting crude product was purified by silica gel column chromatography (chloroform/hexane=1/1) to give 4.19 g (90%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127544
Source datasetuspto-grants-2000_10
ORD IDord-28251f226699450aac1f05d136722b9c
Source noteuspto-grants-2000_10