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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936949Generated: October 25, 2026

Sodium Hydroxide → 5'-(4-Cyano-3-fluorophenyl)-spiro[cyclohexane-1,3'-[3H]indol]-2'(1'H)-one

https://huagongshe.com/reaction/1936949

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantSodium AcetateHCID 517045—
Reactant4-Bromo-2-fluorobenzonitrileHCID 736029—
Reactant(spiro[cyclohexane-1,3'-[3H]indol]-2'(1'H)-one-5-yl)boronic acidHCID 21986219—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Product5'-(4-Cyano-3-fluorophenyl)-spiro[cyclohexane-1,3'-[3H]indol]-2'(1'H)-oneHCID 2201934637%

Reaction Steps

A solution of 4-cyano-3-fluoro-bromobenzene (0.76 g, 3.8 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.3 g) in ethylene glycol dimethyl ether (15 cm3) was stirred under N2 for 20 minutes. To this mixture was then added (spiro[cyclohexane-1,3′-[3H]indol]-2′(1′H)-one-5-yl) boronic acid (1.4 g, 5.7 mmol) and sodium acetate (1.2 g, 11.4 mmol) in water (5 cm3). The solution was brought to reflux for 18 hours and then cooled to room temperature, poured into 2N NaOH and extracted with EtOAc (×3). The combined extracts were washed with water, brine, dried (MgSO4), and evaporated. The residue was purified by column chromatography (SiO2, EtOAc, hexane) to afford the title compound (0.45 g, 37%) as an off-white solid. mp: 258-260° C.; 1H NMR (DMSO-d6) δ8.8 (s, 1H), 7.7-7.6 (m, 2H), 7.5 (td, 2H, J=0.9. 1.5, 5.7 Hz), 7.4 (dd, 1H, J=1.5, 8.8 Hz), 7.0 (d, 1H, J=8.1 Hz), 2.0-1.6 (m, 10H); MS (−)APCI [M−H]− @ m/z 319.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06391907B1
Source datasetuspto-grants-2002_05
ORD IDord-05737275ea4e4e039b2fe66eb62b0cdb
Source noteuspto-grants-2002_05