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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366018Generated: October 30, 2026

Indole → 1-(2,2-Diethoxyethyl)-1H-indole

https://huagongshe.com/reaction/366018

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIndoleHCID 798—
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
ReactantEthane, 2-bromo-1,1-diethoxy-HCID 74852—
SolventDimethyl SulfoxideHCID 679—
Product1-(2,2-Diethoxyethyl)-1H-indoleHCID 22013069—

Reaction Steps

To a solution of 12 g of indole in 100 ml of dimethyl sulfoxide was added 6.5 g of sodium hydride at room temperature. The mixture was stirred at the same temperature for 1 hour, and 20 ml of bromoacetaldehyde diethyl acetal was added thereto, followed by further stirring at 50° C. for 1 hour. After cooling, the reaction mixture was poured into water, and the product was extracted with ethyl ether. The organic layer was dried over anhydrous magnesium sulfate and concentrated to give 23 g of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06127544
Source datasetuspto-grants-2000_10
ORD IDord-c9169fe959ff4a74b13c988b553fd350
Source noteuspto-grants-2000_10