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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1618156Generated: November 2, 2026

4-Methoxyphenol → 1,2-Benzenedicarbonitrile, 4-(4-methoxyphenoxy)-

https://huagongshe.com/reaction/1618156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethoxyphenolHCID 9015—
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Benzenedicarbonitrile, 4-nitro-HCID 97443—
SolventAcetoneHCID 180—
Product1,2-Benzenedicarbonitrile, 4-(4-methoxyphenoxy)-HCID 952085106.2%

Reaction Steps

A mixture of 4-nitro-phthalonitrile (4.00 g), 4-methoxy-phenol (3.46 g) and potassium carbonate (6.39 g) in acetone (64 ml) was heated to reflux for 2 h. Reaction mixture was cooled and filtered. Filtrate was concentrated and the residue was dissolved in ethyl acetate (100 ml). The solution was washed with NaOH (1 N, 50 ml), water, and then brine. The organic layer was dried over magnesium sulfate, filtered, and concentrated to give the product (6.14 g). 1H NMR (200 MHz, CDCl3) δ 6.70 (d, J=7.8 Hz, 1H), 7.21 (m, 2 H), 6.96 (m, 4 H), 3.84 (s, 3 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765956B2
Source datasetuspto-grants-2014_07
ORD IDord-d245c1b0cb4f40a5b67139afe9d35337
Source noteuspto-grants-2014_07