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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428507Generated: October 30, 2026

Ethyl Bromide → 3-(1,4-Dioxa-spiro[4,5]dec-8-yl)-5-cyano-1-ethyl-indole

https://huagongshe.com/reaction/428507

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl BromideHCID 6332—
ReactantSodium hydrideHCID 24758—
Reactant3-(1,4-Dioxa-spiro[4,5]dec-8-yl)-5-cyano-1H-indoleHCID 15521973—
SolventDimethylformamideHCID 6228—
Product3-(1,4-Dioxa-spiro[4,5]dec-8-yl)-5-cyano-1-ethyl-indoleHCID 1841406269%

Reaction Steps

To a suspension of sodium hydride (60%, 1.63 g, 0.068 mol) in anhydrous N,N-dimethylformamide (150 ml) was added 3-(1,4-dioxa-spiro[4,5]dec-8-yl)-5-cyano-1H-indole (9.0 g, 0.032 mol) at room temperature. The mixture was stirred for 30 minutes at room temperature then ethylbromide (14.6 g, 0.13 mol) was added at room temperature. The reaction was allowed to stir for overnight, 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 (hexanes) afforded 5.5 g (69%) of product as a white solid: mp 124-126° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313126B1
Source datasetuspto-grants-2001_11
ORD IDord-3c395166575445e4921e4e861ec071e1
Source noteuspto-grants-2001_11