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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953338Generated: November 3, 2026

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

https://huagongshe.com/reaction/1953338

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 numberUS06114536
Source datasetuspto-grants-2000_09
ORD IDord-0f90e31b9b0746279bc64740b94d7649
Source noteuspto-grants-2000_09