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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066459Generated: November 1, 2026

Water → 1-(tert-butyldimethylsilyl)-5-fluoro-1H-indole

https://huagongshe.com/reaction/2066459

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium hydrideHCID 24758—
Reactanttert-Butyldimethylsilyl chlorideHCID 28928—
Reactant5-FluoroindoleHCID 67861—
SolventTetrahydrofuranHCID 8028—
Product1-(tert-butyldimethylsilyl)-5-fluoro-1H-indoleHCID 59418220—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 5-fluoro-1H-indole (30.0 g, 0.222 mol) in anhydrous THF (250 mL) was added sodium hydride (60% suspension in mineral oil, 10.22 g, 0.255 mol) portionwise and maintaining the solution at 0° C. The reaction mixture was stirred at 0° C. for 20 min, then a solution of tert-butyl-chloro-dimethyl-silane (40.15 g, 0.266 mol) in anhydrous THF (20 mL) was added and the solution stirred at RT for 25 h. The reaction mixture was poured into H2O and the layers separated. The aqueous layer was extracted with EtOAc and the combined organic layers were dried (MgSO4), then concentrated in vacuo. The resultant residue was purified by column chromatography (silica gel, cyclohexane:DCM 100% to 50:50) to provide the title compound was obtained as a colourless oil (41.2 g, 74%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293735B2
Source datasetuspto-grants-2012_10
ORD IDord-c5c36c5bf1f94525b7f14256fbe02601
Source noteuspto-grants-2012_10