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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428506Generated: October 30, 2026

Methyl iodide → 3-(1,4-Dioxa-spiro[4,5]dec-7-en-8-yl)-5-cyano-1-methyl-indole

https://huagongshe.com/reaction/428506

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium hydrideHCID 24758—
Reactant3-(1,4-Dioxaspiro[4.5]dec-7-EN-8-YL)-1H-indole-5-carbonitrileHCID 15521972—
SolventDimethylformamideHCID 6228—
Product3-(1,4-Dioxa-spiro[4,5]dec-7-en-8-yl)-5-cyano-1-methyl-indoleHCID 1841410224.7%

Reaction Steps

To a suspension of sodium hydride (60%, 1.74 g, 0.073 mol) in anhydrous N,N-dimethylformamide (100 ml) was added 3-(1,4-dioxa-spiro[4,5]dec-7-en-8-yl)-5-cyano-1H-indole (9.9 g, 0.035 mol) at room temperature. The mixture was stirred for 30 minutes at room temperature, then methyl iodide (9 ml, 0.14 mol) was added at room temperature. The reaction was allowed to stir for 1 hour, then quenched with water (50 ml). The mixture was extracted with methylene chloride (3×150 ml) and water (3×150 ml). The organic layer was dried over anhydrous magnesium sulfate and filtered. The solvent was removed under vacuum. Chromatography (5% methanol-methylene chloride) afforded 2.54 g (24%) of product as a light yellow solid: mp 65-67° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313126B1
Source datasetuspto-grants-2001_11
ORD IDord-3de975413aac4124a0c3056385fada5c
Source noteuspto-grants-2001_11