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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1475326Generated: November 1, 2026

Diisopropylethylamine → 6-Bromo-5-fluoro-3,3-dimethyl-1-triisopropylsilanyl-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/1475326

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantTriisopropylsilyl trifluoromethanesulfonateHCID 2724529—
Reactant6-bromo-5-fluoro-3,3-dimethyl-2,3-dihydro-1H-indoleHCID 86723947—
SolventDichloromethaneHCID 6344—
Product6-Bromo-5-fluoro-3,3-dimethyl-1-triisopropylsilanyl-2,3-dihydro-1H-indoleHCID 8672394669.2%

Reaction Steps

Triisopropylsilyltrifluoromethanesulfonate (3.5 mL, 13.0 mmol) and DIPEA (3.2 mL, 19.5 mmol) were added to a solution of 6-bromo-5-fluoro-3,3-dimethyl-2,3-dihydro-1H-indole (1.5 g, 6.5 mmol) in DCM (50 mL). The reaction mixture was stirred at room temperature overnight then quenched with saturated aqueous NaHCO3 and extracted with DCM (×3). The organic phase was dried (MgSO4), filtered and concentrated. The crude material was purified by SiO2 chromatography (10% EtOAc in petrol) to give the title compound (1.8 g) as a white solid. 1H NMR (DMSO-d6): 7.07 (1H, d), 6.65 (1H, d), 3.44 (2H, s), 1.64-1.33 (3H, m), 1.33-1.17 (6H, m), 1.10 (18H, d).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09018214B2
Source datasetuspto-grants-2015_04
ORD IDord-963e24db7e9644a190154face561b808
Source noteuspto-grants-2015_04