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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 11037Generated: October 26, 2026

Sodium hydride → 1-(3-{[Tert-butyl(dimethyl)silyl]oxy}propyl)-2-[2-(2-chlorophenyl)ethenyl]-5-methoxy-1h-indole

https://huagongshe.com/reaction/11037

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
Reactant(3-Bromopropoxy)(tert-butyl)dimethylsilaneHCID 607486—
Reactant2-[2-(2-Chlorophenyl)ethenyl]-5-methoxy-1H-indoleHCID 69583801—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product1-(3-{[Tert-butyl(dimethyl)silyl]oxy}propyl)-2-[2-(2-chlorophenyl)ethenyl]-5-methoxy-1h-indoleHCID 69583812—

Reaction Steps

Sodium hydride (1.05 g of a 50% dispersion in mineral oil, 0.022 mol) was added to a solution of the 2-[2-(2-Chlorophenyl)ethenyl]-5-methoxy-1H-indole prepared according to example 37 (4.13 g, 0.014 mol) in DMF (30 mL) and the solution was stirred at room temperature for 5 min. 3-Bromopropyl tert-butyl(dimethyl)silyl ether (4.04 g, 0.016 mol) was added and stirring was continued for 2 h. The solution was diluted with water, extracted with EtOAc which was washed well with brine and the organic phase was dried, the drying agent was removed and the solution was concentrated to dryness to give 1-(3-{[tert-Butyl(dimethyl)silyl]oxy}propyl)-2-[2-(2-chlorophenyl)ethenyl]-5-methoxy-1H-indole (28) as an oily solid (4.98 g) (as a mixture of E/Z isomers) which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07094798B1
Source datasetuspto-grants-2006_08
ORD IDord-4c6ae40223f9402a82a15bbacc3512f7
Source noteuspto-grants-2006_08