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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666852Generated: October 30, 2026

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

https://huagongshe.com/reaction/1666852

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant5-BromoindoleHCID 24905—
ReactantTriisopropylsilyl trifluoromethanesulfonateHCID 2724529—
SolventDimethylformamideHCID 6228—
Product5-Bromo-1-(triisopropylsilyl)-1H-indoleHCID 2794652—

Reaction Conditions

Temperature0 °C

Reaction Steps

Place a 35% oil dispersion of KH (6 g) in a flask under nitrogen, rinse with 50 mL hexanes and dry under vacuum. Cool the solid suspension in 100 mL anhydrous DMF to 0° C. Add dropwise over 10 minutes a solution of 5-bromoindole (10.3 g, 52.5 mmol) in 25 mL DMF. Stir the mixture 1 hour at 0° C. then treat with triisopropylsilyltrifluoromethane sulfonate (32.2 g, 105.1 mmol). Remove the cooling bath and stir the reaction 72 hours before pouring into 500 mL water and extracting with EtOAc. Dilute the combined extracts with hexanes, wash with brine then dry over MgSO4. Concentration under vacuum and chromatograph on silica gel eluting with 1% EtOAc in hexanes to give 5-Bromo-1-triisopropylsilanyl-1H-indole as a colorless oil: 1H NMR (CDCl3) 7.73-7.72 (d, 1H), 7.36-7.34 (d, 1H), 7.24-7.23 (d, 1H), 7.21-7.19 (m, 1H), 6.55-6.54 (m, 1H), 1.72-1.61 (m, 3H), 1.13-1.10 (m, 18H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044090B2
Source datasetuspto-grants-2011_10
ORD IDord-e71336b9b1434ed498fba988262cf4ac
Source noteuspto-grants-2011_10