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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 525840Generated: October 26, 2026

Acetonitrile → Methyl 4-(2,3,6-trichloro-4,5-dicyano-phenoxy)benzoate

https://huagongshe.com/reaction/525840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantMethylparabenHCID 7456—
ReactantPotassium CarbonateHCID 11430—
Reactant1,2-Benzenedicarbonitrile, 3,4,5,6-tetrachloro-HCID 16057—
SolventEthyl AcetateHCID 8857—
ProductMethyl 4-(2,3,6-trichloro-4,5-dicyano-phenoxy)benzoateHCID 117902339—

Reaction Steps

To a 250 mL flask, 4.8 g of tetrachlorophthalonitrile, 3.98 g of methyl 4-hydroxybenzoate, 5 g of potassium carbonate (K2CO3), and 55 mL of acetonitrile are added, followed by heating for 12 hours while refluxing. After completion of the reaction, 30 mL of ethyl acetate is added and filtered to remove the solvent. To the obtained solid, a suitable amount of dichloromethane is added to dissolve the solid, followed by adding hexane for crystallization. The obtained solid is filtered and dried under vacuum to obtain a compound, methyl 4-(2,3,6-trichloro-4,5-dicyano-phenoxy)benzoate. The first step reaction may be represented by Reaction Scheme 1:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09341743B2
Source datasetuspto-grants-2016_05
ORD IDord-91f652bde2d144b8bcc88d059b1c6ca6
Source noteuspto-grants-2016_05