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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6983Generated: October 27, 2026

Potassium Carbonate → 5-(3-Chloro-phenyl)-3,3-dimethyl-1,3-dihydro-indol-2-one

https://huagongshe.com/reaction/6983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant(3-Chlorophenyl)boronic acidHCID 2734323—
Reactant5-bromo-3,3-dimethyl-2,3-dihydro-1H-indol-2-oneHCID 12052796—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
SolventAmmonium ChlorideHCID 25517—
Product5-(3-Chloro-phenyl)-3,3-dimethyl-1,3-dihydro-indol-2-oneHCID 981692125%

Reaction Steps

5-bromo-1,3-dihydro-3,3-dimethyl-2H-indol-2-one (0.98 g, 4.07 mol) and, tetrakis(triphenylphosphine)palladium(0) (0.239 g) were stirred under an atmosphere of nitrogen in dimethoxyethane (35 cm3). After 15 min., 3-chlorophenylboronic acid (1.27 g, 8.13 mol) was added, followed by potassium carbonate (3.40 g, 45 mmol) in water (15 cm3). The reaction was heated to reflux for 2 hours and then stirred at room temperature overnight. The mixture was diluted with sat. ammonium chloride and extracted with EtOAc (×3). The combined organic layers were dried (MgSO4), filtered, and evaporated. The residue was purified by column chromatography (SiO2, EtOAc: hexane, 1:3) to afford the title compound (0.284 g, 25%): mp 188–189° C.; 1H NMR (DMSO-d6) δ 3.34 (s, 6H), 6.93 (d, 1H, J=8.04 Hz), 7.38–7.35 (m, 1H), 7.53–7.43 (m, 2H), 7.61 (d, 1H, J=7.68 Hz), 7.70 (s, 2H), 10.40 (s, 1H); IR (KBr) 3420, 3150, 3050, 1700 cm−1; MS (EI) m/z 270 (M−H)−; Anal. Calc. for C16H14ClNO+0.1C4H8O2: C, 70.21; H, 5.32; N, 4.99; Found: C, 70.3; H, 5.44; N, 4.93.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07084168B2
Source datasetuspto-grants-2006_08
ORD IDord-78f0cb74792a4655a3abe774e955057c
Source noteuspto-grants-2006_08