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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1295178Generated: October 30, 2026

Water → 5-Bromo-1-(triisopropylsilyl)-1H-indole

https://huagongshe.com/reaction/1295178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-BromoindoleHCID 24905—
ReactantTriisopropylsilyl chlorideHCID 139400—
ReactantLithium bis(trimethylsilyl)amideHCID 57426343—
SolventTetrahydrofuranHCID 8028—
Product5-Bromo-1-(triisopropylsilyl)-1H-indoleHCID 279465292%

Reaction Steps

Lithium hexamethyldisilazane [1.0 M] (44.7 mL, 44.4 mmol) was added to a solution of 5-bromo-1H-indole (7.30 g, 37.0 mmol) in tetrahydrofuran (50 mL) at room temperature. After stirring for 5 minutes, triisopropylsilyl chloride (8.62 g, 44.4 mmol) was added to reaction mixture and stirred for 30 minutes. Water was added to quench the reaction and the solvent was removed under reduced pressure to give the crude mixture, which was purified via column chromatography on silica gel (9:1 hexane/ethyl acetate) to give the title compound in 92% yield. 1H NMR (CDCl3) δ 7.74 (d, J=1.8, 1H), 7.36 (d, J=8.8 Hz, 1H), 7.22 (m, 2H), 6.55 (d, J=3.1 Hz, 1H), 1.65 (m, 3H), 1.12 (d, J=7.5 Hz, 18H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241789B2
Source datasetuspto-grants-2007_07
ORD IDord-aa371aada629411ab7e3572636d24420
Source noteuspto-grants-2007_07