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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1719391Generated: November 3, 2026

Sodium hydride → HCID 20268206, compound

https://huagongshe.com/reaction/1719391

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant2H-Pyran, 2-[(8-bromooctyl)oxy]tetrahydro-HCID 170916—
Reactant2-(1-Imidazolyl)-3-methylindoleHCID 13280839—
SolventDimethylformamideHCID 6228—
ProductHCID 20268206HCID 20268206—

Reaction Steps

To a suspension of 3.0 g of 50% sodium hydride in mineral oil in 40 ml of dimethylformamide under nitrogen at 0°-5° is added dropwise over 20 minutes a solution of 10.0 g of 3-methyl-2-(1-imidazolyl)indole in 60 ml of dimethylformamide. The mixture is stirred for 0.5 hour at 0°-5° followed by the dropwise addition of 17.5 g of 1-tetrahydropyranyloxy-8-bromooctane in 50 ml of dimethylformamide. After stirring at 0°-10° for 1 hour and at room temperature for 0.5 hour, the reaction mixture is poured into ice-water and extracted with ether. The ether extract is washed with water, dried over MgSO4 and evaporated to dryness. The residue is dissolved in 100 ml of 3N hydrochloric acid, the resulting mixture is kept at room temperature for 0.5 hour, washed with ether, basified with aqueous 3N sodium hydroxide solution and extracted with methylene chloride. The methylene chloride solution is evaporated to dryness to give 1-(8-hydroxyoctyl)-2-(1-imidazolyl)-3-methylindole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04539410
Source datasetuspto-grants-1985_09
ORD IDord-88dda9fcf46a402eaea0d56e748a55d0
Source noteuspto-grants-1985_09