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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylsilane | HCID 12052 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4,6-difluoro-1H-indole | HCID 2778736 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,6-Difluoro-2,3-dihydro-1H-indole | HCID 16244449 | 90% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889730B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-b625551253404b8c9fa1ac2e381bad55 |
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| Source note | uspto-grants-2014_11 |
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