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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2421233Generated: November 1, 2026

Triethylamine → 6-Ethenyl-1-[3-fluoro-4-(methyloxy)phenyl]-4-(methyloxy)-1H-indole

https://huagongshe.com/reaction/2421233

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-Fluoro-4-methoxyphenylboronic acidHCID 2782194—
Reactant1H-Indole, 6-ethenyl-4-methoxy-HCID 59627918—
CatalystCupric acetateHCID 8895—
SolventDichloromethaneHCID 6344—
Product6-Ethenyl-1-[3-fluoro-4-(methyloxy)phenyl]-4-(methyloxy)-1H-indoleHCID 6713645347.4%

Reaction Steps

To a solution of 6-ethenyl-4-(methyloxy)-1H-indole (D8) (665 mg, 3.84 mmol) in dichloromethane (20 mL) was added 3-fluoro-4-methoxyphenylboronic acid (1.31 g, 7.71 mmol), triethylamine (1.1 mL, 7.91 mmol), copper (II) acetate (1.39 g, 7.68 mmol) and powdered 4A molecular sieves (1.0 g). The reaction mixture was stirred at room temperature in the presence of air for 18 hours. Further quantities of 3-fluoro-4-methoxyphenylboronic acid (330 mg), triethylamine (0.28 mL) and copper acetate (340 mg) were added and the mixture stirred at room temperature in the presence of air for a further 48 hours. The mixture was filtered and the solid washed with dichloromethane. The filtrate was concentrated at reduced pressure. The product was purified by silica gel chromatography eluting with 5-50% dichloromethane in hexane to yield the title compound (D9), (541 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07956083B2
Source datasetuspto-grants-2011_06
ORD IDord-40526b80e805496b8857e00d0b01dabf
Source noteuspto-grants-2011_06