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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 39207Generated: October 25, 2026

Potassium Carbonate → Pentyl 4-(3,4-dicyanophenoxy)benzoate

https://huagongshe.com/reaction/39207

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantPentyl 4-hydroxybenzoateHCID 23019—
Reactant1,2-Benzenedicarbonitrile, 4-nitro-HCID 97443—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
ProductPentyl 4-(3,4-dicyanophenoxy)benzoateHCID 6898126285%

Reaction Conditions

Temperature85 °C

Reaction Steps

A mixture of 4-nitrophthalonitrile (1.00 g, 7 mmol), pentyl 4-hydroxybenzoate (1.45 g, 7 mmol) and dried potassium carbonate (6.38 g, 46.2 mmol) in anhydrous DMF (50 mL) was stirred overnight at 85° C. under argon. After cooling to room temperature, the mixture was diluted with ethyl acetate (60 mL) and water (40 mL). The organic layer was separated, and the aqueous phase was extracted with ethyl acetate (2×50 mL). The combined organic layers were washed with a saturated solution of NaHCO3 (40 mL), brine (40 mL) and dried over anhydrous sodium sulfate. The solvents were removed in vacuo, and the crude product was purified by column chromatography on silica gel using a dichloromethane/acetonitrile mixture (20:1) as an eluent to give the product in 85% yield. [1H NMR (δ, ppm, CDCl3): 8.15 (d, 2H, J=8.7 Hz), 7.77 (d, 1H, J=8.7 Hz), 7.35 (d, 1H, J=2.3 Hz), 7.30 (d, 1H, J=8.7 Hz), 7.12 (d, 2H, J=8.7 Hz), 4.34 (2H, t, OCH2, J=6.7 Hz), 1.79 (m, 2H, CH2), 1.42 (m, 4H, CH2CH2), 0.94 (t, 3H, J=7 Hz, CH3).]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524891B2
Source datasetuspto-grants-2013_09
ORD IDord-55bb5dca550f4cd6ac687da0cbf92ba2
Source noteuspto-grants-2013_09