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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 338227Generated: October 30, 2026

Trifluoroacetic acid → 4,6-Difluoro-2,3-dihydro-1H-indole

https://huagongshe.com/reaction/338227

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantSodium BicarbonateHCID 516892—
Reactant4,6-difluoro-1H-indoleHCID 2778736—
SolventDichloromethaneHCID 6344—
Product4,6-Difluoro-2,3-dihydro-1H-indoleHCID 1624444990%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a suspension of 4,6-difluoro-1H-indole (5 g, 32.9 mmol) in dry dichloromethane (100 mL) was added triethylsilane (10 g, 85.5 mmol) at room temperature. The reaction was then cooled to 0° C. and trifluoroacetic acid (50 mL) was added dropwise. The reaction was stirred at room temperature for 4 hours. The mixture was poured into cold saturated aqueous sodium bicarbonate solution and diluted with dichloromethane (200 mL). The layers were separated and the organic phase was dried over sodium sulfate, concentrated in vacuo, and purified by silica chromatography to give the title compound (4.5 g, 90% yield) as colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08889730B2
Source datasetuspto-grants-2014_11
ORD IDord-b625551253404b8c9fa1ac2e381bad55
Source noteuspto-grants-2014_11