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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016645Generated: October 31, 2026

Calcium Carbonate → 6-Chloro-2-(4-fluorophenyl)-1H-indole

https://huagongshe.com/reaction/1016645

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCalcium CarbonateHCID 10112—
Reactant1-Ethynyl-4-fluorobenzeneHCID 522627—
Reactant5-Chloro-2-iodoanilineHCID 639697—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
CatalystHCID 178418397HCID 178418397—
SolventDiethylamineHCID 8021—
Product6-Chloro-2-(4-fluorophenyl)-1H-indoleHCID 1840703385%

Reaction Steps

A mixture of 5-chloro-2-iodoaniline (33.0 g, 0.13 mol) and 1-ethynyl-4-fluorobenzene (26.4 g, 0.22 mol) in diethylamine (400 mL) was degassed with bubbling nitrogen for 20 min., then tetrakis(triphenylphosphine)palladium(0) (2.0 g, 1.7 mmol) and copper (I) iodide (170 mg, 0.9 mmol) were added and the mixture was stirred at room temperature for 12 h. The solvent was evaporated under reduced pressure, water was added and the mixture was extracted with ethyl acetate. The combined organic fractions were washed with water (2×), dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was dissolved in dimethylformamide (250 mL), calcium carbonate (13 g, 0.13 mol) and copper (I) iodide (12.4 g, 0.07 mol) were added and the mixture was stirred at 120° C. for 22 h. The mixture was cooled, filtered and the solvent was evaporated under reduced pressure. Water was added and the mixture was extracted with ethyl acetate. The combined organic fractions were washed with water (2×) and brine, dried (MgSO4) and the solvent was evaporated under reduced pressure. The residue was triturated with ether/hexane and the solid was collected and dried in vacuo to give the title compound (25.4 g, 85%). 1H NMR (360 MHz, CDCl3) δ 7.59 (2H, m), 7.49 (1H, d, J 8.5 Hz), 7.44 (1H, s), 7.24-6.99 (3H, m), and 6.69 (1H, d, J 1.8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476045B2
Source datasetuspto-grants-2002_11
ORD IDord-4efa7ef293a542eca902132c550cedb2
Source noteuspto-grants-2002_11