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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174570Generated: October 31, 2026

4-Iodophenol → HCID 7694615, compound

https://huagongshe.com/reaction/2174570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-IodophenolHCID 10894—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Bromomethyl)benzonitrileHCID 86996—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 7694615HCID 7694615—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a stirred solution of 4-iodo phenol (620 mg, 3.18 mmol) in acetonitrile (6 ml) was added K2CO3 (1.31 g, 9.54 mmol), followed by 4-cyanobenzyl bromide (700 mg, 3.18 mmol) at 20-35° C. and the reaction mixture was stirred at 80° C. for 6 h. The progress of the reaction was monitored by TLC. After 6 h of stirring, the mixture was cooled to 20-35° C., diluted with water (50 ml) and extracted with ethyl acetate (2×50 ml). The combined organic layers were washed with brine (50 ml), followed by drying over anhydrous Na2SO4 and filtering. The filtrate was rotary evaporated to get residue which was purified by column chromatography using a mixture of 10% ethyl acetate/hexane as an eluent to get the desired compound as a to pale yellow solid (800 mg, 75%). 1H NMR (400 MHz, DMSO-d6) δ 7.86 (d, J=8.3 Hz, 2H), 7.64-7.59 (m, 4H), 6.90-6.85 (m, 2H), 5.21 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062002B2
Source datasetuspto-grants-2015_06
ORD IDord-3086be2b5c234532b79c6f2fba975761
Source noteuspto-grants-2015_06