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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2221233Generated: October 31, 2026

Potassium Carbonate → HCID 22032964, compound

https://huagongshe.com/reaction/2221233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Benzyl-5-Bromo-1H-IndoleHCID 285756—
Reactant3-(Trifluoromethoxy)phenylboronic Acid (contains varying amounts of Anhydride)HCID 2734385—
CatalystTetrabutylammonium BromideHCID 74236—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22032964HCID 2203296438%

Reaction Steps

1-Benzyl-5-[3-(trifluoromethoxy)phenyl]-1H-indole was prepared by coupling 1-benzyl-5-bromo-1H-indole (2.28 g, 7.97 mmol), and 3-(trifluoromethoxy)phenylboronic acid (1.66 g, 8.06 mmol), using potassium carbonate (2.75, 19.9 mmol), palladium (II) acetate (0.0731 g, 0.326 mmol), and tetrabutylammonium bromide (2.78 g, 8.62 mmol) in water (45 mL) and THF (5 mL), according to the procedure described in Step 1 of Example 21. Following work-up the residue was purified by reverse phase HPLC using 81% acetonitrile and 0.1% TFA in water as the mobile phase. Evaporation of the acetonitrile, extraction of the aqueous phase with ethyl acetate, and evaporation to dryness afforded the title compound as an orange solid (1.10 g, 38%), mp: 62-65° C. Mass spectrum (+ESI, [M+H]+) m/z 368.5; 1HNMR (500 MHz, DMSO-d6): δ7.9 (s, 1H), 7.7 (m, 1H), 7.5-7.6 (m, 4H), 7.45 (dd, 1H, J=8.6 Hz and 1.8 Hz), 7.2-7.3 (m, 6H), 6.55 (m, 1H), and 5.45 ppm (s, 1H). Elemental Analysis for C22H16F3NO: Calculated: C, 71.93; H, 4.39; N, 3.81. Found: C, 71.53; H, 4.16; N, 3.79.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07368471B2
Source datasetuspto-grants-2008_05
ORD IDord-120b64e8ff474de294a9cca6941e34c2
Source noteuspto-grants-2008_05